WO2012142604A2 - Ciblage d'une signalisation wnt dérégulée dans le cancer à l'aide d'hélices alpha de bcl-9 stabilisées - Google Patents

Ciblage d'une signalisation wnt dérégulée dans le cancer à l'aide d'hélices alpha de bcl-9 stabilisées Download PDF

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WO2012142604A2
WO2012142604A2 PCT/US2012/033822 US2012033822W WO2012142604A2 WO 2012142604 A2 WO2012142604 A2 WO 2012142604A2 US 2012033822 W US2012033822 W US 2012033822W WO 2012142604 A2 WO2012142604 A2 WO 2012142604A2
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Prior art keywords
bcl9
peptide
cancer
sah
catenin
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PCT/US2012/033822
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WO2012142604A3 (fr
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Loren D. Walensky
Ruben CARRASCO
Gregory H. Bird
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Dana-Farber Cancer Institute, Inc.
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Priority to CN201280029656.5A priority Critical patent/CN103649113B/zh
Application filed by Dana-Farber Cancer Institute, Inc. filed Critical Dana-Farber Cancer Institute, Inc.
Priority to CA2833171A priority patent/CA2833171C/fr
Priority to US14/111,299 priority patent/US10703785B2/en
Priority to EP12771731.2A priority patent/EP2697254B1/fr
Priority to EP18164082.2A priority patent/EP3360892B1/fr
Priority to CN201711420142.3A priority patent/CN108276490B/zh
Priority to EP20172306.1A priority patent/EP3715366A1/fr
Priority to JP2014505404A priority patent/JP2014515748A/ja
Priority to AU2012242502A priority patent/AU2012242502B2/en
Publication of WO2012142604A2 publication Critical patent/WO2012142604A2/fr
Publication of WO2012142604A3 publication Critical patent/WO2012142604A3/fr
Priority to US16/876,779 priority patent/US11220532B2/en
Priority to US17/455,831 priority patent/US20220204572A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/82—Translation products from oncogenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • A61K38/1709—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Definitions

  • ⁇ -catenin a key component of a tightly regulated receptor-mediated signal transduction network required for both embryonic development and adult tissue homeostasis.
  • ⁇ -catcnin binds to adenomatous polyposis coli (APC), glycogen synthase kinase 3 ⁇ (GSK3 ), and Axin, which form a destruction complex that phosphorylates ⁇ -catenin, targeting it for proteosomal degradation.
  • APC adenomatous polyposis coli
  • GSK3 glycogen synthase kinase 3 ⁇
  • Axin Axin
  • LRP5 and LRP6 The binding of Wnt ligands to the frizzled and low-density lipoprotein receptors (LRP5 and LRP6) inhibits the activity of the GSB ⁇ /APC/Axin complex, enabling non-phosphorylated ⁇ -catenin to undergo nuclear translocation to exert its transcriptional effects.
  • Nuclear ⁇ -catenin associates with the lymphoid enhancer factor/T-cell factor (LEF/TCF) family of transcription factors to induce the expression of cell proliferation, migration, and survival genes, such as c-Myc and cyclin Dl. Normally, this transcriptional pathway is turned off when Wnt ligands uncouple from their receptors.
  • LEF/TCF lymphoid enhancer factor/T-cell factor
  • the transcriptional activity of ⁇ -catenin further depends on two co-factors, BCL9 and Pygopus.
  • BCL9 The formation of a quaternary complex consisting of TCF, ⁇ -catenin, BCL9, and Pygopus enhances ⁇ -catenin- dependent Wnt transcriptional activity.
  • the human BCL9 gene was first identified by cloning the t(l;14)(q21;q32) translocation from a patient with precursor B-cell acute lymphoblastic leukemia (ALL). Amplifications of the chromosome lq21- locus in which the BCL9 gene resides is observed in a broad range of human cancer types and it has been associated with tumor progression, decreased survival and poor clinical outcome.
  • ALL B-cell acute lymphoblastic leukemia
  • BCL9-mediated enhancement of ⁇ -catenin's transcriptional activity increases cell proliferation, migration, invasion, and the metastatic potential of tumor cells by promoting the loss of an epithelial phenotype and gain of a mesenchyme-like functionality.
  • shRNA- induced downregulation of BCL9 in vivo suppresses the expression of Wnt targets c- Myc, cyclin Dl, CD44, and VEGF, and correspondingly increases the survival of xenograft mice with CRC and MM by reducing tumor load, metastasis, and the host angiogenesis response.
  • the Wnt pathway consists of a tightly regulated receptor-mediated signal transduction system required for both embryonic development and adult tissue homeostasis in vertebrates and invertebrates and involves canonical and non- canonical Wnt pathways.
  • TSG tumor suppressor genes
  • oncogenes in a wide range of common human cancers including colorectal, hepatocellular, breast, endometrial carcinomas and MM.
  • the canonical Wnt pathway has been implicated in the regulation of normal (e.g., wound healing) as well as pathological processes (e.g., diabetes).
  • Such mechanisms would result in a method of treatment of cancer cells with SAH-BCL9 and result in inhibition of tumor cell proliferation, migration, tumor-induced angiogenesis, tumor load, de-differentiation (epithelial-mesenchymal transition [EMT]), and metastasis in Wnt/ -catenin-driven cancers.
  • EMT epidermal-mesenchymal transition
  • the invention provides structurally-constrained, protease-resistant, and cell- permeable BCL9 ⁇ -helical peptides, and methods of use of those peptides as therapeutic and prophylactic agents.
  • Such structurally-constrained peptides display excellent proteolytic, acid, and thermal stability, and possess superior
  • the peptides of the invention are stabilized with at least one hydrocarbon staple, but could include two, three or more hydrocarbon staples. The inclusion of multiple hydrocarbon staples
  • hydrocarbon staples is particularly suited for alpha helical peptides that are 20 or more amino acids in length.
  • the hydrocarbon staples allow for the amino acid residues on an interacting face to be properly oriented due to stabilization of the helical structure of the BCL9 HD2 domain.
  • the invention provides a structurally constrained peptide of an
  • HD2 domain of BCL9 (BCL9- HD2), comprising at least one hydrocarbon staple or stitch.
  • the peptide comprises an interacting face comprised of amino acids that interact with ⁇ -catenin.
  • the interacting face comprises about 3 to about 20 amino acids.
  • the interacting face comprises 4-15 amino acids. In various embodiments, the interacting face comprises 40% or greater identity to a helical face of BCL9-HD2 that binds ⁇ -catenin, wherein the interacting face comprises BCL9 residues Gln-355, His-358, Arg-359, Ser-362, Leu-363, Leu- 366, rie-369, Gln-370, Leu-373, and Phe-374, or conservative substitutions thereof.
  • the interacting face comprises 50% to 90% identity to the helical face of BCL9-HD2 that binds ⁇ -catenin, wherein the interacting face comprises BCL9 residues Gln-355, His-358, Arg-359, Ser-362, Leu-363, Leu-366, Ile-369, Gln-370, Leu-373, and Phe-374, or conservative substitutions thereof.
  • the interacting face represents a single face of an a- helix.
  • the single face of a helix comprises one, two, three, or four adjacent stacked columns of amino acids, wherein the stacked columns of amino acids are defined by positions a, d, and g; positions b and e; or positions c and f; in an alpha helix having 3.6 amino acids per turn wherein the amino acids are consecutively and serially assigned positions a-g; and positions a and d; positions b and e; or positions c and f in a 3 io helix having 3 amino acids per turn wherein the amino acids are consecutively and serially assigned positions a-f; or homologues thereof.
  • the invention provides a structurally constrained peptide consisting of: between about 20% to 100% sequence homology to amino acids 351 to 374 of BCL9-HD2, SEQ ID NO: 1
  • the invention provides a structurally constrained peptide consisting of: between about 50% to 100% sequence homology to amino acids 351 to 374 of BCL9-HD2, SEQ ID NO: 1
  • the peptide comprises between one and five hydrocarbon staples
  • the hydrocarbon staple or stitch is between one or more natural or non-natural amino acids.
  • the hydrocarbon staple or stitch is formed by an olefin metathesis reaction.
  • the non-natural amino acids are selected from following:
  • the structurally constrained peptide comprises 1 to 5 staples or stitches within the BCL9 HD2 peptide.
  • one staple or stitch is located at the following positions within the BCL9 HD2 peptide: a) i, i+4; b) i, i+7; and c) i, i+3.
  • another staple or stitch is located at the following positions within the BCL9 HD2 peptide: a) i, i+4; b) i, i+7; and c) i, i+3.
  • any other staples or stitches are located at the following positions within the BCL9 HD2 peptide: a) i, i+4; b) i, i+7; and c) i, i+3.
  • the invention provides a structurally constrained peptide, wherein one hydrocarbon staple is located at the following exemplary positions within the BCL9 HD2 peptide, and iterated by staple scanning:
  • the invention provides a structurally constrained peptide, wherein two hydrocarbon staples are located at the following exemplary positions within the BCL9 HD2 peptide, and iterated by staple scanning:
  • the invention provides a structurally constrained peptide, wherein the one or more hydrocarbon staples or stitches is located at any of the following exemplary positions within the BCL9 HD9 domain and iterated by staple scanning:
  • the invention provides a structurally constrained peptide, further comprising one to four additional hydrocarbon staples.
  • the invention provides a structurally constrained peptide, wherein the additional hydrocarbon staples are located at any of the following exemplary positions within the BCL9 HD2 domain and iterated by staple scanning:
  • amino acid sequence of positions 351 to 374 is selected from the following:
  • SEQ ID NO: 1 BCL9 HD2 domain: LSQEQLEHRERSLQTLRDIQRMLF
  • SEQ ID NO:2 BCL9 HD2 domain M372B LSQEQLEHRERSLQTLRDIQRBLF
  • SEQ ID NO:3 SAH-BCL9 A : LSQEQLEHRERSLQTLRXIQRXLF
  • SEQ ID NO:4 SAH-BCL9 B : LSQEQLEHRERSLXTLRXIQRBLF
  • SEQ ID NO:5 SAH-BCL9 C : LSQEQLEHREXSLQXLRDIQRBLF
  • SEQ ID NO:6 SAH-BCL9 B (H358D): LSQEQLEDRERSLXTLRXIQRBLF
  • SEQ ID NO:7 SAH-BCL9 B (R359E): LSQEQLEHEERSLXTLRXIQRBLF
  • the invention provides a composition comprising the peptide as described above and a pharmaceutically acceptable carrier.
  • the invention further provides a peptide of the invention in a pharmaceutical carrier in a unit dosage form.
  • the invention provides a method of inhibiting canonical Wnt/p-catenin signaling in a subject, comprising administering a peptide of the invention.
  • the invention provides a method of inhibiting binding of BCL9 to ⁇ -catenin in a subject, comprising administering a peptide of the invention.
  • the inhibition of binding of BCL9 to ⁇ -catenin is caused by the structurally constrained peptide of the invention.
  • the invention provides a method of treating a disease or disorder mediated by BCL9/P-catenin binding in a subject, comprising administering to the subject a peptide of the invention.
  • the subject has been identified as being in need of an inhibitor of the BCL9/p-catenin interaction or Wnt signaling.
  • the disease is cancer, tumor cell proliferation, tumor cell de-differentiation and metastasis, tumor migration, tumor induced angiogenesis, cancer stem cell chemoresistance, and a proliferation disease; or involves wound healing, angiogenesis or diabetes.
  • the invention provides methods for the amelioration or treatment of cancer, for example in a subject, by administration of a structurally-constrained peptide of the invention to the subject in a therapeutically effective amount.
  • the method can further include one or more of identifying a subject as being in need of amelioration or treatment of cancer, or monitoring the subject for the prevention, amelioration, or treatment of cancer.
  • the invention provides methods of amelioration or treatment of cancer where in the subject is identified as being in need of BCL9/ -catenin modulation.
  • the disease is colorectal cancer, multiple myeloma, lung cancer, colon cancer, breast cancer, prostate cancer, liver cancer, pancreas cancer, brain cancer, kidney cancer, ovarian cancer, stomach cancer, skin cancer, bone cancer, gastric cancer, breast cancer, pancreatic cancer, glioma, gliobastoma, hepatocellular carcinoma, papillary renal carcinoma, head and neck squamous cell carcinoma, leukemias, lymphomas, myelomas, and solid tumors.
  • the invention provides a method of treating cancer in a subject, comprising administering to the subject a peptide of the invention.
  • the subject has been previously identified as in need of a canonical Wnt/ -catenin signaling inhibitor to treat the cancer.
  • the disease involves wound healing, angiogenesis or diabetes.
  • the subject is administered with an additional therapeutic agent, radiation or chemotherapy.
  • the additional therapeutic compound is an anticancer compound.
  • the compound and the additional therapeutic agent are administered simultaneously or sequentially.
  • the compound and the additional therapeutic agent are linked together (ie. a bifunctional compound).
  • the subject is a human.
  • the invention provides a kit comprising a structurally constrained peptide of the invention and instructions for use in treating cancer.
  • the invention provides a method of identifying a compound that inhibits binding of BCL9 to ⁇ -catenin, comprising the steps of contacting the peptide of the invention with ⁇ -catenin and then screening for small molecules or compounds that disrupt the interaction between the peptide of the invention and ⁇ - catenin.
  • FIG. 1 Design, synthesis, and characterization of SAH-BCL9 peptides, a.
  • SAH-BCL9 A-C were generated by replacing native residues on the non-interacting surface of the HD2 domain with olefinic non-natural amino acids, which when subjected to olefin metathesis yield the corresponding stapled peptides.
  • An unmodified template peptide (BCL9 HD2) was also generated, c.
  • TCL total cellular lysate.
  • FITC-SAH- BCL9 B and ⁇ -catenin preferentially localize to the nucleus of Colo320 cells as monitored by confocal microscopy and cellular fractionation analyses, g.
  • H358D and R359E reverse polarity mutants of FITC-SAH-BCL9 B exhibited similar high percent oc-helicity compared to the wild-type SAH by CD analysis, h.
  • Point mutagenesis impaired FITC-SAH-BCL9/ -catenin co-immunoprecipitation, with the R359E- derivative serving as the most effective negative control, i.
  • FITC-SAH-BCL9s and its R359E control exhibit dose-equivalent cellular uptake by Colo320 cells.
  • SAH-BCL9 # disrupts native P-catenin-BCL9/B9L complexes and represses Wnt p-catenin/BCL9-driven transcription.
  • SAH-BCL9 B dose- responsively disrupted the association of ⁇ -catenin with BCL9 and B9L, whereas cellular treatment with SAH-BCL9B(R359E) had no effect.
  • Dissociation of ⁇ -catenin from BCL9 B9L correlated with the co-immunoprecipitation of ⁇ -catenin with FITC- SAH-BCL9 S .
  • Colo320 cells were transfected with TOP-FLASH, incubated with vehicle or SAH-BCL9 peptides and assayed for luciferase activity, which was normalized to Renilla luciferase control.
  • SAH-BCL9 Bi but not SAH-BCL9 B (R359E)
  • Wnt-dependent reporter activity Error bars are mean +/- s.d. for assays performed in triplicate.
  • qPCR analysis revealed repression of the Wnt target genes VEGF, c-Myc and Axin2, but not GAPDH, in response to SAH-BCL9 B treatment.
  • Vehicle and SAH-BCL9 B (R359E) had no effect.
  • SAH-BCL9 B but not vehicle or SAH-BCL9 B (R359E), likewise impaired the growth of MM IS cells in the presence or absence of Wnt3A-conditioned medium (Wnt3A- CM) and multiple myeloma primary tumors (MMPT). *, P ⁇ 0.01.
  • SAH-BCL9 B had no effect on the viability of Colo320 and MM IS cells as assessed by CellTiter- Glo at 72 h.
  • SAH-BCL9 B did not activate caspase-3 or PA P, as monitored by western analysis, g. SAH-BCL9 B treatment decreased VEGF secretion by Colo320 and MM 1S cells as measured by ELISA.
  • HUVEC were cultured with supernatants collected from Colo320 or MM IS cells incubated with vehicle or SAH-BCL9 B peptides and the number of tubes (black arrows) formed per high power field analyzed by microscopy at 5 h.
  • SAH-BCL9 B blocked the migration of Colo320 cells as monitored using Matrigel Boy den chambers. Vehicle and SAH-BCL9B(R359E) had no effect.
  • SAH-BCL9 S inhibits tumor growth, angiogenesis, and metastasis in vivo.
  • a. Cohorts (n - 6) of NOD/SCID mice bearing intraperitoneal GFP-positive Colo320 cells were treated with vehicle (2.5 % DMSO in D5W) or SAH-BCL9 B peptides (20 mg/kg) administered intraperitoneally every other day for a total of six doses.
  • vehicle 2.5 % DMSO in D5W
  • SAH-BCL9 B peptides (20 mg/kg) administered intraperitoneally every other day for a total of six doses.
  • Whole body imaging and necropsy revealed decreased tumor burden and liver metastases in SAH-BCL9 B -treated mice but not in vehicle- and SAH-BCL9 B (R359E)- treated animals, b.
  • FIG. 5 Targeting Wnt transcriptional activity in cancer using Stabilized Alpha-Helices of BCL9.
  • Deregulated Wnt signaling underlies the pathogenesis of a broad range of human cancers yet the development of targeted therapies to disrupt the pathway has remained a challenge
  • ⁇ -catenin is a central effector of the canonical Wnt pathway, activating the expression of genes such as c-Myc, cyclin Dl, VEGF, and CD44 that are involved in cell proliferation, migration, and angiogenesis.
  • BCL9 is an important co-activator for ⁇ -catenin-mediated transcription, and is highly expressed in tumors but not in the cells of origin, presenting an opportunity to selectively inhibit pathologic ⁇ -catenin activity.
  • Stabilized Alpha-Helices of BCL9 were generated to block Wnt signaling in cancer through targeted disruption of the BCL9/ -catenin complex.
  • SAH-BCL9 reduces Wnt transcriptional activity and the expression of Wnt/ -catenin transcriptional targets, impeding tumor cell proliferation, migration, invasion, and angiogenesis in vitro and in vivo.
  • Figure 6 BCL9 is overexpressed in a broad range of tumors.
  • FITC-SAH- BCL9 B and FITC-SAH-BCL9 B exhibit equivalent temperature- dependent uptake in Colo320 cells, consistent with the energy-dependent endocytic uptake mechanism previously documented for stapled peptides (Bernal, F., et al. J Am Chem Soc 129, 2456-7 (2007); Walensky, L. D. et alScience 305, 1466-70 (2004)).
  • FITC-SAH-BCL9B and FITC-SAH-BCL9 B (R359E) peptides exhibit equivalent cellular uptake by Colo320 and MM1S cells.
  • SAH-BCL9 B selectively engages ⁇ -catenin and does not disrupt its interaction with a non-BCL9 binding partner, a.
  • ⁇ -catenin targeting by FITC-SAH-BCL9 B is selective for disruption of the BCL9/3-catenin complex and does not affect anti- -catenin co-immunoprecipitation of E-cadherin from MCF7 cell lysates. b.
  • MCF7 cells Treatment of MCF7 cells with FITC-SAH-BCL9 B followed by anti-FITC pulldown performed on cellular lysates revealed the selective interaction between FITC-SAH-BCL9 B and ⁇ -catenin, and no coimmunoprecipitation of unrelated proteins such as IxBa and actin.
  • Single R359E point mutagenesis of the SAH-BCL9 binding interface abrogates co-immunoprecipitation of ⁇ -catenin, further confirming the specificity of the SAH-BCL9 B peptide.
  • MCF7 cells were employed in this assay as they contain readily detectable levels of E-cadherin protein for monitoring the ⁇ - catenin/E-cadherin interaction.
  • Figure 9 Treatment of MCF7 cells with FITC-SAH-BCL9 B followed by anti-FITC pulldown performed on cellular lysates revealed the selective interaction between FITC-SAH-BCL9 B and ⁇ -caten
  • HCTl 16 cells transfected with TOP-FLASH and pcDNA-BCL9 were treated with vehicle or SAH- BCL9 peptides (5 ⁇ ) and dual luciferase assays were performed at 24 h.
  • the suppression of reporter activities by SAH-BCL9 B is dose-responsively reversed by increasing BCL9 protein expression, highlighting the on-target specificity of SAH- BCL9 B -based inhibition of -cs&etim/BCL9-dnven transcription.
  • *P ⁇ 0.01. HCTl 16 cells were employed in this assay due to their relatively low level expression of endogenous BCL9.
  • VEGF is a direct transcriptional target of BCL9.
  • Chromatin immunoprecipitation analysis (ChIP) of Colo320 cells using anti-TCF-4, ⁇ -catenin, and BCL9 antibodies documented that, like c-Myc, the VEGF promoter is a target of the Wnt/ -catenin BCL9 transcriptional complex.
  • Negative controls included ChIP with IgG and the use of primers to a non-specific, upstream region of the VEGF promoter.
  • Colo320 cells lentivirally transduced with control shRNA or BCL9 shRNA vector were transfected with VEGF promoter-luciferase reporter plasmids. Reporter activity was assayed using the dual lucif erase assay system and results normalized to Renilla values for each sample. BCL9 knockdown effectively decreased transcriptional activity at the VEGF promoter.
  • FIG. 12 Normal appearance of colonic mucosa and bone marrow in SAH- BCL9-treated mice. H&E staining of colonic mucosa and bone marrow tissues isolated from experimental mice treated with vehicle or SAH-BCL9-peptides showed no evidence of toxicity across all histologic specimens.
  • SAH-BCL9B inhibits the proliferation of INA-6 multiple myeloma cells
  • Figure 14 Examples of non-natural olefinic amino acids inserted into peptide templates to generate hydrocarbon-stapled peptides by olefin metathesis.
  • Figure 15. Examples of singly-, doubly-, and sequentially stapled BCL9 HD2 peptides.
  • X stapling amino acid;
  • B norleucine.
  • a staple scan readily enables iterative production and testing of distinct staple compositions and their differential positions along the peptide sequence to identify optimally stabilized alpha-helix of BCL9 HD2 constructs.
  • Figure 16 Three dimensional structure of residues 351-374 of the a-helical HD2 domain of BCL9, highlighting those amino acid residues of the BCL9 HD2 interaction face that contact ⁇ -catenin.
  • SAH-BCL9 B disrupts P-catenin-BCL9/B9L complexes
  • a Differential binding affinities of SAH-BCL9 B and SAH-BCL9 B (R359E) for recombinant ⁇ - catenin.
  • R359E SAH-BCL9 B dose-responsively dissociated recombinant -catenin/BCL9 complexes as demonstrated by GST-pull-down assay.
  • R359E point mutagenesis reduced SAH-BCL9 B activity by 6-fold.
  • SAH-BCL9 B selectively blocks Wnt transcription
  • qRT-PCR analysis revealed dose-dependent repression of Wnt target genes in response to SAH-BCL9 B treatment of Colo320 cells. Error bars are mean +/- s.d. for assays performed in quadruplicate. * p ⁇ 0.01. Quantitative comparison of genes down-regulated by SAH- BCL9 B and dominant-negative TCF1/TCF4 expression in DLDl cells across adenoma (b) and carcinoma (c) signatures.
  • FIG. 19 Suppression of Wnt target gene expression by SAH-BCL9 B .
  • SAH-BCL9 £ selectively inhibits proliferation of cultured colon cancer cells that are driven by pathologic Wnt signaling and express BCL9.
  • SAH- BCL9 B but not vehicle or SAH-BCL9,v/c/r, significantly reduced the proliferation of CRC cell lines.
  • SAH-BCL9 B -susceptible cancer cells express BCL9, whereas the LS174T cell line that does not express BCL9 showed no response, linking the inhibitory effect of SAH-BCL9 B with BCL9 expression.
  • HCT116 cells and its two derivative cell lines, HCT116DO20 and HCT116K058, whose proliferative capacity does not depend on Wnt/ -catenin activity showed no sensitivity to SAH-BCL9 B .
  • Colo320 cells were co-cultured with vehicle, SAH- BCL9 B, or SAH-BCL9 M t / r and increasing concentrations of 5-fluorouracil (5-FU), and evaluated for cellular proliferation using 3 H-thymidine incorporation, b.
  • MM IS cells were co-cultured with vehicle, SAH-BCL9 B, or SAH-BCL9,vit / r and increasing concentrations of doxorubicin (Dox), and evaluated for cellular proliferation using 3 H-thymidine incorporation.
  • SAH-BCL9 S but not SAH-BCL9MC / T or vehicle significantly enhanced the an ti- tumor activity of the conventional agents.
  • FIG 22 Increased apoptosis in colonic tumor tissue of SAH-BCL9s-treated mice.
  • Tumor tissue of NOD/SCID mice bearing intraperitoneal Colo320 cells were evaluated for apoptosis induction using TUNEL assay (brown).
  • Three representative 40X power fileds are shown, including quantitation of TUNEL positivity in 6 high power fields. * p ⁇ 0.001.
  • FIG. 23 Proliferation of INA-6 cells is dependent on Wnt transcriptional activity and increased apoptosis in myeloma tumor tissue of SAH-BCLi -treated mice.
  • INA-6 cells were lentivirally transduced with empty vector (Mock) or a vector expressing a dominant negative form of TCF4 (EdTP) and proliferation was measured by 3 H-thymidine incorporation
  • b Tumor tissue sections from NOD/SCED mice bone chips bearing INA-6 cells were evaluated for apoptosis induction using TUNEL assay (brown).
  • SAH-BCL9 B but not vehicle or or SAH-BCL9 Mi/ r, notably increased TUNEL positivity.
  • Three representative 40X power fileds are shown, including quantitation of TUNEL positivity in 6 high power fields. * p ⁇ 0.001. DETAILED DESCRIPTION
  • the crystal structure of the P-catenin/BCL9/TCF-4 complex revealed that the BCL9 binding site on ⁇ -catenin is distinct from other binding partners in that the a- helical HD2 domain of BCL9 (residues 352-374) binds a surface groove formed by a- helices 2 and 3 of the armadillo repeat 1 of ⁇ -catenin (Fig. la) (Sampietro, J. et al. Mol Cell 24, 293-300 (2006)).
  • alanine mutagenesis of key residues at the BCL9 binding interface such as H358A or R359A, blocked the ability of BCL9 to bind ⁇ -catenin, abrogating transactivation.
  • Circular dichroism (CD) analysis confirmed that hydrocarbon stapling consistently enhanced peptide -helicity compared to the corresponding unmodified peptide (BCL9 HD2) (Fig. lc).
  • Both FITC and ⁇ -catenin immunoprecipitation identified SAH-BCL9g as the most effective ⁇ -catenin interactor in situ (Fig. Id).
  • SAH-BCL9 B and its corresponding R359E mutant were selected for functional studies in the ⁇ - catenin/BCL9-dependent cell lines Colo320 and MM1S (Mani, M. et al. Cancer Res 69, 7577-86 (2009); Ilyas, M., et al. Proc Natl Acad Sci U S A 94, 10330-4 (1997)), which display dose-equivalent uptake of the two peptides (Fig. li).
  • FITC-SAH-BCL9 but not SAH-BCL9 B (R359E), dose-responsively co-immunoprecipitated with ⁇ -catenin (Fig. 2a), linking ⁇ -catenin targeting by SAH-BCL9 B with disengagement of the ⁇ - catenin-BCL9/B9L complexes.
  • FiTC-SAH-BCL9 B had no effect on ⁇ -catenin's homeostatic interaction with E-cadherin, consistent with the distinct, non-overlapping location of the BCL9 ⁇ -catenin binding site.
  • the target-based selectivity of FITC-SAH-BCL9 B was further documented by anti-FITC pulldown, which co-precipitates ⁇ -catenin but not other unrelated cellular proteins such as ⁇ and actin.
  • Quantitative PCR (qPCR) analysis was employed to measure the effects of vehicle, SAH-BCL9 B , and SAH-BCL9 B (R359E) on the expression of P-catenin/BCL9 target genes, including VEGF.
  • SAH-BCL9 B but not vehicle or SAH-BCL9 B (R359E)
  • significantly • reduced mRNA levels of VEGF, c-Myc, and Axin2 but not GAPDH, a non-Wnt pathway target gene (Fig. 2c).
  • Colo320 and MM IS cells were treated with vehicle and SAH-BCL9 B peptides and then VEGF levels were quantitated in the media. Consistent with the qPCR analysis, only SAH-BCL9 B reduced the level of secreted VEGF (Fig. 3g).
  • human umbilical vein endothelial cells (HUVEC) were cultured with supernatants from treated Colo320 or MM IS cells and then scored for the formation of capillary tube-like formations by microscopy.
  • HUVEC cells exposed to the supernatant from SAH-BCL9 B -treated cells showed reduced capillary tube formation compared to the vehicle- and SAH-BCL9 B (R359E)-treated controls (Fig. 3h).
  • SAH-BCL9 S also decreased the adhesive and invasive potential of Colo320 cells, as reflected by a significant reduction in the capacity of SAH-BCL9 B -treated cells to pass thorough the extracellular matrix, as evaluated using Matrigel-coated invasion chambers (Fig. 3i).
  • GFP-expressing Colo320 cells (lxlO 6 ) were injected into the peritoneum of sublethally irradiated NOD/SCID mice. Two days after cellular injection, mouse cohorts (n - 6) were treated with vehicle (2.5 % DMSO in D5W), SAH-BCL9 S , or SAH-BCL9s(R359E) peptides (20 mg/kg) for a total of 6 doses administered intraperitoneally every other day.
  • mice were sacrificed and evaluated for tumor burden and metastasis by whole body imaging and histologic examination of harvested GFP-positive tissues.
  • Overall tissue fluorescence was markedly reduced in mice treated with SAH-BCL9 B compared to vehicle and SAH- BCL9 fl (R359E)-treated animals (Fig. 4a).
  • Fig. 4b-c mice were sacrificed and evaluated for tumor burden and metastasis by whole body imaging and histologic examination of harvested GFP-positive tissues.
  • Fig. 4a mice treated with SAH-BCL9 B compared to vehicle and SAH- BCL9 fl (R359E)-treated animals.
  • Fig. 4a tumor tissue from SAH-BCL9s- treated mice also showed decreased tumor cell CD44 immunoreactivity (Fig. 4b), a reduction in the number of intratumoral blood vessels (Fig. 4d), and less intense capillary CD34 immunoreactivity (Fig.
  • vehicle 2.5 % DMSO in D5W
  • SAH-BCL9 B SAH-BCL9 B
  • R359E SAH-BCL9 B
  • mice were sacrificed 33 days after INA-6 cell injection and evaluated for MM tumor burden by fluorescence imaging, histologic analysis, and anti-CD34 staining. Consistent with the measured levels of shuIL-6R, tumor burden within the bone chip was significantly reduced in SAH- BCL9 fl -treated mice (Fig. 4g-h). Interestingly, the tumor cells present in SAH- BCL9a-treated mice resided within the confines of the bone chip, whereas vehicle- and SAH-BCL9 f i(R359E)-treated mice demonstrated invasion into the surrounding soft tissue (Fig. 4h, black arrows).
  • SAH-BCL9B- treated SCID-hu mice Similar to the CRC model, local angiogenesis was suppressed in SAH-BCL9B- treated SCID-hu mice, as monitored by anti-CD34 staining and blood vessel quantitation (Fig. 4i).
  • SAH-BCL9 effectively suppressed tumor growth, invasion, and angiogenesis in a sequence-specific manner.
  • the ⁇ -catenin transcriptional complex is a high priority pharmacologic target due to its pathologic role in a broad range of cancers. Because ⁇ -catenin participates in a variety of homeostatic functions and engages the majority of its interaction partners using the same binding surface (Barker, N. & Clevers, H. Nat Rev Drug Discov 5, 997-1014 (2006)), achieving anti-cancer activity and selectivity remains a pressing challenge.
  • PKFl 15-584 a small molecule identified by high- throughput screening for inhibitors of the ⁇ -catenin/TCF interaction, blocked Wnt- specific transcriptional activity and reduced the growth of colon cancer cells (Lepourcelet, M. et al.
  • the invention is based, at least in part, on the results provided herein, as well as PCT/US2009/000438 (WO 2009/108261; filed January 23, 2009) demonstrating that stabilized alpha helical peptides have excellent structural, proteolytic, acid, and thermal stability. It has also been determined that stabilized alpha helical peptides are highly effective in interfering with Wnt ⁇ -catenin signaling, indicating that the peptide can be used for the treatment of cancer.
  • the stabilized alpha-helical peptides have superior pharmacologic properties in vivo compared to their unmodified counterparts, reducing the frequency and quantity of stabilized alpha-helical peptide that needs to be administered as compared to a native peptide sequence, and ensuring that exposure is sustained.
  • stabilizing crosslink shall refer to its namesake or other covalent, or ionic, crosslink such as, but not limited to, a disulfide, amide, ester, 1,2,3-triazole, or other bioconjugate or biocompatible crosslink.
  • hydrocarbon-staple or “hydrocarbon- crosslink” or derivation thereof, shall refer to its namesake or other hydrocarbon covalent, or ionic, bioconjugate or biocompatible crosslinks.
  • the alpha helix HD2 domain is stabilized with at least one molecular tether, e.g., hydrocarbon staple, but may include two, three or more hydrocarbon staples.
  • hydrocarbon staple e.g., hydrocarbon staple
  • the inclusion of multiple hydrocarbon staples is particularly suited for alpha helical peptides that are 16 or more amino acids in length.
  • the inclusion of more than one (e.g., 2, 3, 4, 5, depending on the length of the peptide) hydrocarbon staples provides for exceptional proteolytic, structural, acid and thermal stability of the modified polypeptides, yielding bioactive peptides with strikingly enhanced pharmacologic properties in vivo (ref Bird et al, PNAS, 2010).
  • the HD2 domain is structurally constrained by one or more modifications of the native sequence.
  • the alpha-helix of the HD2 domain can be stabilized using a molecular tether such as a hydrocarbon staple.
  • amino acid substitutions can be made in or adjacent to the region to include natural or non-natural amino acids to promote the desired structure of the peptide, to promote or maintain the desired angle between the two helices or to orient the helices relative to each other, or to improve the pharmacologic properties.
  • at least one of the helices of the HD2 domain includes a molecular tether such as a hydrocarbon staple to promote or maintain the helical nature of the domain.
  • both of the helices of the HD2 domain include a molecular tether(s) such as hydrocarbon staple(s) to promote or maintain the helical nature of the domain. Hydrocarbon stapling of Polypeptides
  • the alpha helix or HD2 domain is stabilized with at least one hydrocarbon staple.
  • Hydrocarbon staples suitable for use with any of the modified polypeptides are described herein and in U.S. Publication Nos. 2005/0250680, 2010/0234563, 2007/0197772, 2006/0008848, 2006/0014675; U.S. Patent Nos. 7,723,469, 7,192,713, and 7,084,244; International Publication Nos. WO 2009/108261) and WO 2010/148335; and Kawamoto, S.A. et al, J. Med. Chem. 55, 1137-1146 (2012); Mahon, A.B. and Arora, P.S., Chem. Commun.
  • Hydrocarbon stapling allows a polypeptide, predisposed to have a helical secondary structure, to maintain its native helical conformation and increase its stability and efficacy.
  • the modified polypeptide has at least 10%, 20%, 30%, 35%, 40%, 45%, 50%, 60%, 70%, 80%, or 90% or more helicity in an aqueous solution as determined by circular dichroism. Assays for determining circular dichroism are known in the art and described herein.
  • the hydrocarbon stapled polypeptides include a tether (linkage) between two amino acids, in which the tether significantly enhances the helical secondary structure of the polypeptide.
  • the tether extends across the length of one or two helical turns (i.e., 3, 4 or 7 amino acids).
  • amino acids positioned at i and i+3; i and i+4; or i and i+7 are ideal candidates for chemical modification and cross- linking.
  • any of the amino acid residues of the modified polypeptides of the invention may be tethered (e.g., cross-linked) in conformity with the above. Suitable tethers are described herein and in U.S. Publication Nos.
  • the hydrocarbon staple(s) is positioned so as to link a first amino acid (i) and a second amino acid (i+3) which is 3 amino acids downstream of the first amino acid.
  • modified polypeptides of the invention will generally include the structure of Formula (I), ( ⁇ ) or (III) provided below.
  • any of the modified polypeptides described herein can be present in a composition (e.g., pharmaceutical composition) or kit.
  • the composition or kit comprises two or more modified polypeptides.
  • the modified polypeptides of the invention include the HD-2 peptides (amino acids 352 to 374 of the following SEQ ID NO: 1 : BCL9 HD2 domain: LSQEQLEHRERSLQTLRDIQRMLF SEQ ID NO:2: BCL9 HD2 domain M372B: LSQEQLEHRERSLQTLRDIQRBLF
  • SEQ ID NO:3 SAH-BCL9 A : LSQEQLEHRERSLQTLRXIQRXLF
  • SEQ ID NO:4 SAH-BCL9 B : LSQEQLEHRERSLXTLRXIQRBLF
  • SEQ ID NO:5 SAH-BCL9 C : LSQEQLEHREXSLQXLRDIQRBLF
  • SEQ ID NO:6 SAH-BCL9 B (H358D): LSQEQLEDRERSLXTLRXIQRBLF
  • SEQ ID NO:7 SAH-BCL9 B (R359E): LSQEQLEHEERSLXTLRXIQRBLF
  • HD2 domain analogs refers to a peptide that is recognized or identified as having a repeat-analog domain or BCL9 domain.
  • Methods for repeat- analog polypeptides are known in the art, for example, bioinformatics programs based on pairwise residue correlations (e.g., on the world wide web at: ch.embnet.org/software/COILS_form.html), which have the ability to recognize coils from protein sequences and model their structures (See Lupas, A., et al. Science 1991.
  • the amino acid substitutions may be of a conserved or non-conserved nature.
  • conserved amino acid substitutions consist of replacing one or more amino acids of the HD2 peptide sequence with amino acids of similar charge, size, and/or hydrophobicity characteristics.
  • Non-conserved substitutions consist of replacing one or more amino acids of the HD2 domain sequence with amino acids possessing dissimilar charge, size, and/or hydrophobicity characteristics.
  • Substitutions can include the use of conserved or non-conserved non-natural amino acids.
  • Amino acid insertions may consist of single amino acid residues or stretches of residues.
  • the insertions may be made at the carboxy or amino terminal end of the full-length or truncated HD2 domain or BCL9 peptide, as well as at a position internal to the peptide. Such insertions will generally range from 2 to 15 amino acids in length. It is contemplated that insertions made at either the carboxy or amino terminus of the peptide of interest may be of a broader size range, with about 2 to about 50 amino acids being preferred. One or more such insertions may be introduced into full- length or truncated HD2 domain or BCL9 peptide, as long as such insertions result in modified peptides which may still exhibit anti-cancer activity.
  • Deletions of full-length or truncated HD2 domain or BCL9 peptide are also within the scope of the invention. Such deletions consist of the removal of one or more amino acids from the HD2 domain or BCL9 peptide; or HD2 domain or BCL9 peptide-like peptide sequence, with the lower limit length of the resulting peptide sequence being 4, 5, or 6 amino acids. Such deletions may involve a single contiguous or greater than one discrete portion of the peptide sequences. One or more such deletions may be introduced into full-length or truncated HD2 domain or BCL9 peptide, as long as such deletions result in peptides which may still exhibit anti-cancer activity.
  • the interaction between the hydrocarbon-stapled peptide and its target protein form a complex in which, on the peptide there can be defined, an interacting face and a non-interacting face. Mutations along the non-interacting face can be made facilely, whilst mutations on the interacting face are not tolerated, such that the residues on the interacting face are the main component of the complex and as such should be conserved and maintained in designed hydrocarbon-stapled peptides. As such, greater than 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of the residues on the interacting face of BCL9 HD2 domain in the -catenin BCL9 complex should unchanged or changed to a structurally or chemically similar amino acid residue. Stabilization of HD2 domain and BCL9 peptides
  • the modified polypeptides of the present invention are structurally constrained (e.g., stabilized, stapled) helical and/or include one or more amino acid sequence modifications as compared to the native (i.e., wild type or otherwise naturally occurring) sequence to incorporate natural and/or non-natural amino acids to limit the structural flexibility of the peptide as compared to the native sequence, which loses bioactive shape when taken out of physiologic context.
  • the polypeptides include at least one molecular tether such as a hydrocarbon staple. Hydrocarbon stapling is described in U.S. Publication Nos. 2005/0250680, 2010/0234563, 2007/0197772, 2006/0008848, 2006/0014675; U.S. Patent Nos.
  • the peptide a-helix participates in critically important protein interactions by presenting specific amino acid residues in an ordered and precise arrangement over a relatively large contact surface area (Chittenden, T., et al, Embo Journal, 1995. 14(22): p. 5589-5596; Kussie, P.H., et al. Science, 1996. 274(5289): p. 948-953; Ellenberger, T.E., et al, Cell, 1992. 71(7): p. 1223-1237).
  • Alpha-helical domains and other protein structural features are frequently stabilized by scaffold sequences in the remainder of the protein, which facilitate the formation and/or maintenance of a helical structure, e.g., an a-helical structure.
  • cc-helical peptide motifs When taken out of context, oc-helical peptide motifs can unfold, leading to loss of biological activity.
  • Critical challenges in developing cc-helical peptides include promoting and/or maintaining their natural ⁇ x- helical structure and preparing peptides that can resist proteolytic, acid and thermal degradation, and thereby remain intact in vivo.
  • Hydrocarbon stapling refers to a process for stably cross-linking a polypeptide via at least two substituted amino acids (or a non-native linkage, e.g., carbon-carbon, from two natural amino acids) that helps to conformationally bestow the native secondary structure of that polypeptide. Hydrocarbon stapling promotes and maintains an alpha-helical secondary structure in peptides that thermodynamically favor an alpha-helical structure. This secondary structure increases resistance of the polypeptide to proteolytic cleavage and heat, and also may increase hydrophobicity.
  • substituted amino acids or a non-native linkage, e.g., carbon-carbon, from two natural amino acids
  • hydrocarbon stapled (structurally constrained, e.g., crosslinked) polypeptides described herein have improved biological activity relative to a corresponding non-hydrocarbon stapled (not structurally constrained) polypeptide.
  • the cross-linked polypeptides described herein can be used therapeutically, e.g., to treat cancer.
  • the hydrocarbon stapled polypeptides include a tether (linkage) between two amino acids, which tether significantly enhances the helical secondary structure of the polypeptide.
  • the tether extends across the length of one or two helical turns (i.e., about 3-3.6 or about 7 amino acids).
  • amino acids positioned at i and i+3; i and i+4; or i and i+7 are ideal candidates for chemical modification and cross-Unking.
  • a peptide has the sequence . . . XI, X2, X3, X4, X5, X6, X7, X8, X9 . . .
  • cross-links between XI and X4, or between XI and X5, or between XI and X8 are useful as are cross-links between X2 and X5, or between X2 and X6, or between X2 and X9, etc.
  • the use of multiple cross-links e.g., 2, 3, 4 or more has also been achieved, compounding the benefits of individual stapled adducts (e.g., improved helicity and activity; improved helicity and thermal stability; improved helicity and acid stability; improved helicity and pharmacologic properties).
  • the use of "stitched" cross-links has also been achieved whereby double linkages are made from a common origin (e.g., XI, X5, and X9, where X5 is the anchor point for both staples).
  • the invention encompasses the incorporation of one or more crosslinks within the polypeptide sequence to either further stabilize the sequence or faciUtate the structural stabiUzation, proteolytic resistance, thermal stability, acid stability, pharmacologic properties, and biological activity enhancement of longer polypeptide stretches.
  • the tethers e.g., hydrocarbon staples are used to stabilize structures other than helices.
  • the ends of the tethers can be placed at intervals other than at i, i + 3, i + 4, and i + 7.
  • modified polypeptides of the invention have the formula (I), O O
  • each Ri and R 2 are independently H or a Ci to Cio alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heteroarylalkyl, or heterocyclylalkyl;
  • R3 is alkyl, alkenyl, alkynyl; [R4--K-- R4] n ; each of which is substituted with 0-6 R5;
  • R4 IS alkyl, alkenyl, or alkynyl
  • R 5 is halo, alkyl, OR 6 , N(R 6 ) 2 , SR 6 , SOR 6 , S0 2 R 6 , CO 2 R6, Re, fluorescent moiety, or a radioisotope;
  • K is O, S, SO, S0 2 , CO, C0 2 , CONR 6 , or
  • R6 is H, alkyl, or a therapeutic agent
  • n is an integer from 1-4;
  • x is an integer from 2-10;
  • each y is independently an integer from 0-100;
  • z is an integer from 1-10 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10);
  • each Xaa is independently an amino acid.
  • the modified polypeptides may include an amino acid sequence which forms an alpha-helix and is 30% or more identical to, an amino acid sequence of SEQ ID NO: 1-7; wherein X is any amino acid and further identifies the amino acid residues which are linked by a hydrocarbon staple, and B is norleucine.
  • the tether can include an alkyl, alkenyl, or alkynyl moiety (e.g., C5, Cs or Cn alkyl or a C 5, Cs or Ci 1 alkenyl, or C5, Cs or Cn alkynyl).
  • the tethered amino acid can be alpha disubstituted (e.g., C1-C3 or methyl).
  • x is 2, 3, or 6. In some instances, each y is independently an integer between 3 and 15.
  • each y is independently an integer between 1 and 15.
  • R t and R 2 are each independently H or Ci-C 6 alkyl.
  • Ri and R 2 are each independently C 1 -C3 alkyl.
  • At least one of Ri and R 2 are methyl.
  • Ri and R 2 are both methyl.
  • R3 is alkyl (e.g., Cg alkyl) and x is 3.
  • R3 is Cn alkyl and x is 6.
  • R3 is alkenyl (e.g., C 8 alkenyl) and x is 3.
  • x is 6 and R3 is Cn alkenyl.
  • R3 is a straight chain alkyl, alkenyl, or alkynyl.
  • the two alpha, alpha disubstituted stereocenters are both in the R configuration or S configuration (e.g., i, i+4 cross-link), or one stereocenter is R and the other is S (e.g., i, i+ 7 cross-link).
  • the C and C" disubstituted stereocenters can both be in the R configuration or they can both be in the S configuration, for example when X is 3.
  • X is 3.
  • the C disubstituted stereocenter is in the R configuration and the C" disubstituted stereocenter is in the S configuration.
  • the R3 double bond may be in the E or Z stereochemical configuration.
  • R3 is [R4--K— RJ n i and R4 is a straight chain alkyl, alkenyl, or alkynyl.
  • the modified polypeptide comprises at least 3, 4, 5, 6, 7, 8, 9, 10, 1 1, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 45, 50, or more amino acids of a repeat or repeat like domain, e.g., a BCL9 HD2 domain.
  • Each [Xaa]y is a peptide that can independently comprise at least 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25 or more amino acids of a repeat or repeat like domain, e.g., a HD2 domain.
  • [Xaa] x is a peptide that can comprise 3 or 6 amino acids of a repeat or repeat like domain.
  • the modified polypeptide can comprise 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50 or more amino acids of a repeat or repeat like domain, e.g., a HD2 domain, e.g., a polypeptide having the amino acid sequence of SEQ ID NO: 1-7, wherein two amino acids that are separated by two, three, or six amino acids are replaced by amino acid substitutes that are linked via R 3 .
  • at least two amino acids can be replaced by tethered amino acids or tethered amino acid substitutes.
  • [Xaa] y - and [Xaa] y - can each comprise polypeptide sequences from the same or different heptad repeat or heptad repeat like domains.
  • the invention features cross-linked polypeptides comprising 10 (11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, 50 or more) amino acids of a repeat or repeat like domain, e.g., a HD2 domain e.g., a polypeptide having the amino acid sequence of SEQ ID NO: 1-7 wherein the alpha carbons of two amino acids that are separated by two, three, or six amino acids are linked via R3, one of the two alpha carbons is substituted by Ri and the other is substituted by R2 and each is linked via peptide bonds to additional amino acids.
  • a repeat or repeat like domain e.g., a HD2 domain
  • a polypeptide having the amino acid sequence of SEQ ID NO: 1-7 wherein the alpha carbons of two amino acids that are separated by two, three, or six amino acids are linked via R3, one of the two alpha carbons is substituted by Ri and the other is substituted by R2 and each is linked via peptide bonds to additional amino acids
  • modified polypeptides of the invention have the formula ( ⁇ ),
  • each Ri and R2 are independently H, alkyl, alkenyl, alkynyl, arylalkyl,
  • cycloalkylalkyl cycloalkylalkyl; heteroarylalkyl; or heterocyclylalkyl;
  • each n is independently an integer from 1-15;
  • x 2, 3, or 6
  • each y is independently an integer from 0-100;
  • z is an integer from 1-10 (e.g., 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10);
  • each Xaa is independently an amino acid.
  • modified polypeptides of the invention have the formula (III),
  • each Ri and R2 are independently H, alkyl, alkenyl, alkynyl, arylalkyl,
  • cycloalkylalkyl cycloalkylalkyl, heteroarylalkyl, or heterocyclylalkyl
  • R3 is alkyl, alkenyl, alkynyl; [R4— K— R4] n or a naturally occurring amino acid side chain; each of which is substituted with 0-6 R5;
  • R4 IS alkyl, alkenyl, or alkynyl
  • R 5 is halo, alkyl, OR 6 , N(R 6 ) 2 , SR 6 , SOR 6 , S0 2 R 6 , CO 2 Re, Re, a fluorescent moiety, or a radioisotope;
  • K is O, S, SO, S0 2 , CO, C0 2 , CONR 6 , or
  • Re is H, alkyl, or a therapeutic agent
  • R 7 is alkyl, alkenyl, alkynyl; [R 4 — K-R4] n or an naturally occurring amino acid side chain; each of which is substituted with 0-6 R 5 ;
  • n is an integer from 1-4;
  • x is an integer from 2-10;
  • each y is independently an integer from 0-100;
  • z is an integer from 1-10 (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10);
  • each Xaa is independently an amino acid.
  • stitched peptides which are disclosed at least at PCT/US2008/058575 (WO 2008/121767), the contents of which are incorporated herein by reference.
  • modified polypeptides may include an amino acid sequence that forms an alpha-helix and is 20% or more identical to, or contain at least 7 amino acids from an amino acid sequence, or at least two amino acids from a face of a helix formed by a peptide having the sequence of SEQ ID NO: 1-7; wherein X is any amino acid and further identifies the amino acid residues which are linked by a hydrocarbon staple, and B is norleucine.
  • modified polypeptides may include an amino acid sequence that forms an alpha-helix and is 30% or more identical to a peptide having the sequence of SEQ ID NO: 1-7.
  • the amino acid sequence in the alpha-helix is 40%, 50%, 60%, 70%, 80%, 90%, or 95% or greater identical to a peptide having the sequence of SEQ ID NO: 1-7.
  • the tether can include one or more of an ether, thioether, ester, amine, or amide moiety.
  • a naturally occurring amino acid side chain can be incorporated into the tether.
  • a tether can be coupled with a functional group such as the hydroxyl in serine, the thiol in cysteine, the primary amine in lysine, the acid in aspartate or glutamate, or the amide in asparagine or glutamine. Accordingly, it is possible to create a tether using naturally occurring amino acids rather than using a tether that is made by coupling two non-naturally occurring amino acids. It is also possible to use a single non-naturally occurring amino acid together with a naturally occurring amino acid.
  • the length of the tether can be varied. For instance, a shorter length of tether can be used where it is desirable to provide a relatively high degree of constraint on the secondary structure, whereas, in some instances, it is desirable to provide less constraint on the secondary structure, and thus a longer tether may be desired. It is further understood that the insertion of the tether at a site or in an amino acid sequence when the amino acid sequence has no tendency to form a helix will not result in helix formation.
  • tethers spanning from amino acids i to i+3, i to i+4; and i to i+7 have been described in order to provide a tether that is primarily on a single face of the alpha helix, the tethers can be synthesized to span any combinations of numbers of amino acids to promote and/or maintain the structures other than alpha helices.
  • the peptides of this invention can be made by chemical synthesis methods, which are well known to the skilled artisan and described herein. See, for example, Fields et al, Chapter 3 in Synthetic Peptides: A User's Guide, ed. Grant, W. H. Freeman & Co., New York, N.Y., 1992, p. 77; and Bird, G. H., et al., Methods Enzymol 446, 369-86 (2008).
  • peptides can be synthesized using the automated Merrifield techniques of solid phase synthesis with the alpha-NH 2 protected by either t-Boc or Fmoc chemistry using side chain protected amino acids on, for example, an Applied Biosystems Peptide Synthesizer Model 430A or 431 or the AAPPTEC multichannel synthesizer APEX 396.
  • SPPS solid phase peptide synthesis
  • the C-terminal amino acid is attached to a cross-linked polystyrene resin via an acid labile bond with a linker molecule.
  • This resin is insoluble in the solvents used for synthesis, making it relatively simple and fast to wash away excess reagents and by-products.
  • the N-terminus is protected with the Fmoc group, which is stable in acid, but removable by base. Any side chain functional groups are protected with base stable, acid labile groups.
  • peptides can also be made by conjoining individual synthetic peptides using native chemical ligation. Alternatively, longer synthetic peptides can be synthesized by well known recombinant DNA techniques. Such techniques are provided in well-known standard manuals with detailed protocols.
  • a coding sequence is made, typically by synthesizing oligonucleotides which encode the peptide and any regulatory elements, if necessary.
  • the coding sequence is inserted in a suitable cloning vector and transfected into a host cell. Furthermore, the host cell is engineered so as to be able to incorporate the non- natural amino acids for the hydrocarbon staple.
  • the peptide is then expressed under suitable conditions appropriate for the selected expression system and host. See Liu et al. Proc. Nat. Acad. Sci (USA), 94: 10092-10097 (1997).
  • the peptide is purified and characterized by standard methods.
  • the peptides can be made in a high-throughput, combinatorial fashion, e.g., using a high-throughput multichannel combinatorial synthesizer such as that available from Advanced Chemtech/APPTTEC, Thuramed or CEM. Definitions
  • agent is understood herein to include a therapeutically active compound or a potentially therapeutic active compound.
  • An agent can be a previously known or unknown compound.
  • an agent is typically a non-cell based compound, however, an agent can include a biological therapeutic agent, e.g., peptide or nucleic acid therapeutic, cytokine, etc.
  • Amelioration or “treatment” is understood as meaning to lessen or decrease at least one sign, symptom, indication, or effect of a specific disease or condition. Amelioration and treatment can require the administration of more than one dose of an agent, either alone or in conjunction with other therapeutic agents and interventions. Amelioration or treatment do not require that the disease or condition be cured.
  • amino acid refers to a molecule containing both an amino group and a carboxyl group.
  • Suitable amino acids include, without limitation, both the D- and L-isomers of the 20 common naturally occurring amino acids found in peptides (e.g., A, R, N, C, D, Q, E, G, H, I, L, K, M, F, P, S, T, W, Y, V (as known by the one letter abbreviations)) as well as the naturally occurring and non-naturally occurring amino acids including beta-amino acids and ⁇ , ⁇ disubstituted amino acids, prepared by organic synthesis or other metabolic routes and that can be applied for specialized uses such as increasing chemical diversity, functionality, binding capacity, structural mimesis, and stability.
  • amino acid side chain or “amino acid R group” refers to a moiety attached to the a-carbon in an amino acid.
  • amino acid side chain or R group for alanine is methyl
  • amino acid side chain for phenylalanine is phenylmethyl
  • amino acid side chain for cysteine is thiomethyl
  • amino acid side chain for aspartate is carboxymethyl
  • amino acid side chain for tyrosine is 4- hydroxyphenylmethyl, etc.
  • non-naturally occurring amino acid side chains are also included, for example, those that occur in nature (e.g., an amino acid metabolite) or those that are made synthetically (e.g., an alpha, alpha di-substituted amino acid, a beta-amino acid).
  • control samples include, for example, cells in culture, one or more laboratory test animals, or one or more human subjects. Methods to select and test control samples are within the ability of those in the art.
  • An analyte can be a naturally occurring substance that is characteristically expressed or produced by the cell or organism or a substance produced by a reporter construct (e.g, ⁇ -galactosidase or luciferase). Depending on the method used for detection the amount and measurement of the change can vary. Determination of statistical significance is within the ability of those skilled in the art.
  • Co-administration as used herein is understood as administration of one or more agents to a subject such that the agents are present and active in the subject at the same time. Co-administration does not require a preparation of an admixture of the agents or simultaneous administration of the agents.
  • a “conservative amino acid substitution” is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain.
  • families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine).
  • amino acid side chain families such as when substituting an asparagine for aspartic acid in order to modify the charge of a peptide.
  • a predicted amino acid residue in a HD2 domain peptide is preferably replaced with another amino acid residue from the same side chain family or homologues across families (e.g., asparagine for aspartic acid, glutamine for glutamic acid).
  • Conservative changes can further include substitution of chemically homologous non-natural amino acids (i.e., a synthetic non- natural hydrophobic amino acid in place of leucine, a synthetic non-natural aromatic amino acid in place of tryptophan).
  • Contacting a cell is understood herein as providing an agent to a test cell e.g., a cell to be treated in culture or in an animal, such that the agent or isolated cell can interact with the test cell or cell to be treated, potentially be taken up by the test cell or cell to be treated, and have an effect on the test cell or cell to be treated.
  • the agent or isolated cell can be delivered to the cell directly (e.g., by addition of the agent to culture medium or by injection into the cell or tissue of interest), or by delivery to the organism by an enteral or parenteral route of administration for delivery to the cell by circulation, lymphatic, or other means.
  • detecting As used herein, “detecting”, “detection” and the like are understood that an assay performed for identification of a specific analyte in a sample, a product from a reporter construct in a sample, or an activity of an agent in a sample.
  • diagnosing refers to a clinical or other assessment of the condition of a subject based on observation, testing, or circumstances for identifying a subject having a disease, disorder, or condition based on the presence of at least one sign or symptom of the disease, disorder, or condition.
  • diagnosing using the method of the invention includes the observation of the subject for other signs or symptoms of the disease, disorder, or condition.
  • ERTAIN amount refers to that amount of an agent to produce the intended pharmacological, therapeutic or preventive result.
  • the pharmacologically effective amount results in the amelioration of one or more signs or symptoms of a disorder provided herein, or prevents the spread of the disorder.
  • a therapeutically effective amount preferably refers to the amount of a therapeutic agent that decreases the rate of cancer spread, by at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or more as compared to an untreated control subject. More than one dose of an agent may be required to provide an effective dose.
  • the terms "effective” and “effectiveness” includes both pharmacological effectiveness and physiological safety. Pharmacological effectiveness refers to the ability of the treatment to result in a desired biological effect in the patient.
  • Physiological safety refers to the level of toxicity, or other adverse physiological effects at the cellular, organ and/or organism level (often referred to as side-effects) resulting from administration of the treatment.
  • side-effects the term “ineffective” indicates that a treatment does not provide sufficient pharmacological effect to be therapeutically useful, even in the absence of deleterious effects, at least in the unstratified population. (Such a treatment may be ineffective in a subgroup that can be identified by the expression profile or profiles.) "Less effective” means that the treatment results in a therapeutically significant lower level of pharmacological effectiveness and/or a therapeutically greater level of adverse physiological effects.
  • a drug which is "effective against" a disease or condition indicates that administration in a clinically appropriate manner results in a beneficial effect for at least a statistically significant fraction of patients, such as a improvement of symptoms, a cure, a reduction in disease signs or symptoms, extension of life, improvement in quality of life, or other effect generally recognized as positive by medical doctors familiar with treating the particular type of disease or condition.
  • the "face" of a helix is understood as the amino acids that are "stacked" in a helix of a protein so that when the helix is positioned vertically, the amino acids in a single face are depicted as being one on top of the other.
  • an alpha-helix has about 3.6 amino acids per turn.
  • amino acid b the second amino acid
  • amino acid b will "stack" with the fifth and sixth amino acids, i.e., amino acids e and f at the +3 and +4 positions, and with amino acid b' at the + 7 position to form a face of the helix.
  • Faces on helices starting with amino acid c, d, e, f, and g can be readily determined based on the above disclosure.
  • a face of a helix can include two adjacent, three adjacent, or four adjacent columns of "stacked" residues.
  • An example of a "face” of a helix includes the "interacting face” of the helix.
  • An "interacting face” amino acid residue is a residue that makes contact with one or more helices in the helix bundle, results in abolishing or substantially abolishing the polypeptide functional activity. Substantially abolishing is understood as reducing the functional activity of a BCL9 peptide to less than about 50%, less than about 40%, less than about 30% of the wild-type peptide in an appropriate assay.
  • the interacting face amino acid residues of the BCL9 peptides can readily be determined by methods well known in the art and are described herein.
  • an essential amino acid residue is in the "a” or “d” position of a BCL9 HD2 domain, while nonessential amino acids may occur in a "b", “c", “e”, “f or “g” position.
  • interacting face” amino acid residue includes conservative substitutions of the interacting face amino acids that do not disrupt function of the sequence. Generally, the "interacting face” amino acid residues are found at the interacting face of the alpha helix.
  • the BLC9, BCL9-like, and HD2 domain and HD2 domain analogs are readily identifiable by those possessing ordinary skill in the art by sequence based homology, structural homology and/or functional homology. Such methods are well known in the art and include bioinformatics programs based on pairwise residue correlations (e.g., ch.embnet.org/software/COILS_form.html), which have the ability to recognize coils from protein sequences and model their structures (See Lupas, A., et al. Science 1991. 252(5009); p. 1162-1164).
  • the modified polypeptide of the invention is 20% or more similar at the interacting face to the amino acid sequence of SEQ ID NO: 1-7. In another embodiment, the modified polypeptide of the invention is 30% or more similar at the interacting face to the amino acid sequence of SEQ ID NO: 1-7. In another embodiment, the modified polypeptide of the invention is 40% or more similar at the interacting face to the amino acid sequence of SEQ ID NO: 1-7. In another embodiment, the modified polypeptide of the invention is 50% or more similar at the interacting face to the amino acid sequence of SEQ ID NO: 1-7. In another embodiment, the modified polypeptide of the invention is 60% or more similar at the interacting face to the amino acid sequence of SEQ ID NO: 1-7.
  • the modified polypeptide of the invention is 70% or more similar at the interacting face to the amino acid sequence of SEQ ID NO: 1-7. In another embodiment, the modified polypeptide of the invention is 80% or more similar at the interacting face to the amino acid sequence of SEQ ID NO: 1-7. In another embodiment, the modified polypeptide of the invention is 90% or more similar at the interacting face to the amino acid sequence of SEQ ID NO: 1-7.
  • the interacting face of BCL9 peptide can be the ⁇ -catenin interacting face.
  • the "interacting face" of the alpha helix includes those amino acid residues which interact with other amino acid residues on other proteins and/or in other helices. Methods for identifying repeats and the interacting face residues are well known in the art and described herein.
  • hydrocarbon stapling refers to a process for stably cross-linking a polypeptide having at least two amino acids that helps to conformationally bestow the native secondary structure of that polypeptide. Hydrocarbon stapling promotes or maintains a helical secondary structure in a peptide predisposed to have a helical secondary structure, e.g., alpha-helical secondary structure, to attain or maintain its native alpha-helical conformation. This secondary structure increases resistance of the polypeptide to proteolytic cleavage and heat, and also may increase hydrophobicity.
  • the hydrocarbon stapled polypeptides include one or more tethers (linkages) between two non-natural amino acids (or a non-native linkage, e.g., carbon-carbon, from two natural amino acids), which tether significantly enhances the helical secondary structure of the polypeptide.
  • the tether extends across the length of one or two helical turns (i.e., about 3, 4, or 7 amino acids).
  • amino acids positioned at i and i+3; i and i+4; or i and i+7 are ideal candidates for chemical modification and cross-linking.
  • a peptide has the sequence . . .
  • cross-links between XI and X4, or between XI and X5, or between XI and X8 are useful as are cross-links between X2 and X5, or between X2 and X6, or between X2 and X9, etc.
  • the use of multiple cross-links (e.g., 2, 3, 4 or more) is also contemplated. The use of multiple cross-links is effective at stabilizing and optimizing the peptide, especially with increasing peptide length.
  • the use of "stitched" cross-links has also been achieved whereby double linkages are made from a common origin (e.g., XI, X5, and X9, where X5 is the anchor point for both staples).
  • a common origin e.g., XI, X5, and X9, where X5 is the anchor point for both staples.
  • the invention encompasses the incorporation of one or more crosslinks within the polypeptide sequence.
  • the use of multiple cross-links is effective at stabilizing and optimizing the peptide, especially with increasing peptide length.
  • the invention encompasses the incorporation of one or more crosslinks within a polypeptide sequence, including stitched crosslinks in which two staples arise from a common origin.
  • the term "staple scan” refers to the synthesis of a library of stapled peptides whereby the location of the i and i+3; i and i+4; and i and i+7 single and multiple staple, or stitches, are positioned sequentially down the length of the peptide sequence, sampling all possible positions, to identify desired or optimal properties and activities for the stapled or stitched constructs.
  • identity refers to the subunit sequence similarity between two polymeric molecules, e.g., two polynucleotides or two polypeptides. When a subunit position in both of the two molecules is occupied by the same monomeric subunit, e.g., if a position in each of two peptides is occupied by serine, then they are identical at that position.
  • the identity between two sequences is a direct function of the number of matching or identical positions, e.g., if half (e.g., 5 positions in a polymer 10 subunits in length), of the positions in two peptide or compound sequences are identical, then the two sequences are 50% identical; if 90% of the positions, e.g., 9 of 10 are matched, the two sequences share 90% sequence identity.
  • the identity between two sequences is a direct function of the number of matching or identical positions. Thus, if a portion of the reference sequence is deleted in a particular peptide, that deleted section is not counted for purposes of calculating sequence identity.
  • Identity is often measured using sequence analysis software e.g., BLASTN or BLASTP (available at (www.ncbi.nih.gov/BLAST).
  • BLASTN sequence analysis software
  • BLASTP for protein sequences
  • isolated or purified when used in reference to a polypeptide means that a natural polypeptide or protein has been removed from its normal physiological environment (e.g., protein isolated from plasma or tissue) or is synthesized in a non-natural environment (e.g., artificially synthesized in an in vitro translation system or using chemical synthesis).
  • an "isolated” or “purified” polypeptide can be in a cell-free solution or placed in a different cellular environment (e.g., expressed in a heterologous cell type).
  • isolated when used in reference to a cell means the cell is in culture (i.e., not in an animal), either cell culture or organ culture, of a primary cell or cell line. Cells can be isolated from a normal animal, a transgenic animal, an animal having spontaneously occurring genetic changes, and/or an animal having a genetic and/or induced disease or condition.
  • kits are understood to contain at least one non-standard laboratory reagent for use in the methods of the invention.
  • a kit can include at least one of, preferably at least two of at least one peptide, and instructions for use, all in appropriate packaging.
  • the kit can further include any other components required to practice the method of the invention, as dry powders, concentrated solutions, or ready to use solutions.
  • the kit comprises one or more containers that contain reagents for use in the methods of the invention; such containers can be boxes, ampules, bottles, vials, tubes, bags, pouches, blister-packs, or other suitable container forms known in the art.
  • Such containers can be made of plastic, glass, laminated paper, metal foil, or other materials suitable for holding reagents.
  • non-essential amino acid residue is a residue that can be altered from the wild-type sequence of a polypeptide without abolishing or substantially altering its activity/secondary structure (alpha-helical structure). "Obtaining” is understood herein as manufacturing, purchasing, or otherwise coming into possession of.
  • operably linked is understood as joined, preferably by a covalent linkage, e.g., joining an amino-terminus of one peptide to a carboxy terminus of another peptide, in a manner that the two or more components that are operably linked either retain their original activity, or gain an activity upon joining such that the activity of the operably linked portions can be assayed and have detectable activity using at least one of the methods provided in the examples.
  • pharmaceutically acceptable carrier includes a pharmaceutically acceptable material, composition or vehicle, suitable for administering compounds of the present invention to mammals.
  • the carriers include liquid or solid filler, diluent, excipient, solvent or encapsulating material, involved in carrying or transporting the subject agent from one organ, or portion of the body, to another organ, or portion of the body.
  • Each carrier must be “acceptable” in the sense of being compatible with the other ingredients of the formulation and not injurious to the patient.
  • pharmaceutically acceptable carriers for administration of cells typically is a carrier acceptable for delivery by injection, and do not include agents such as detergents or other compounds that could damage the cells to be delivered.
  • materials which can serve as pharmaceutically acceptable carriers include: sugars, such as lactose, glucose and sucrose; starches, such as corn starch and potato starch; cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients, such as cocoa butter and suppository waxes; oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols, such as propylene glycol; polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; esters, such as ethyl oleate and ethyl laurate; agar; buffering agents, such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer'
  • wetting agents such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, release agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the compositions.
  • antioxidants examples include: water soluble antioxidants, such as ascorbic acid, cysteine hydrochloride, sodium bisulfate, sodium metabisulfite, sodium sulfite and the like; oil-soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, a-tocopherol, and the like; and metal chelating agents, such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid, and the like.
  • water soluble antioxidants such as ascorbic acid, cysteine hydrochloride, sodium bisulfate, sodium metabisulfite, sodium sulfite and the like
  • oil-soluble antioxidants such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin
  • Formulations of the present invention include those suitable for oral, nasal, topical, transdermal, buccal, sublingual, intramuscular, intraperotineal, rectal, vaginal and/or parenteral administration.
  • the formulations may conveniently be presented in unit dosage form and may be prepared by any methods well known in the art of pharmacy.
  • the amount of active ingredient that can be combined with a carrier material to produce a single dosage form will generally be that amount of the compound that produces a therapeutic effect.
  • plurality is understood to mean more than one.
  • a plurality refers to at least two, three, four, five, or more.
  • a "polypeptide” or “peptide” as used herein is understood as two or more independently selected natural or non-natural amino acids joined by a covalent bond (e.g., a peptide bond).
  • a peptide can include 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more natural or non-natural amino acids joined by peptide bonds.
  • Polypeptides as described herein include full length proteins (e.g., fully processed proteins) as well as shorter amino acids sequences (e.g., fragments of naturally occurring proteins or synthetic polypeptide fragments).
  • sample refers to a biological material that is isolated from its environment (e.g., blood or tissue from an animal, cells, or conditioned media from tissue culture) and is suspected of containing, or known to contain an analyte, such as a virus, an antibody, or a product from a reporter construct.
  • a sample can also be a partially purified fraction of a tissue or bodily fluid.
  • a reference sample can be a "normal" sample, from a donor not having the disease or condition fluid, or from a normal tissue in a subject having the disease or condition (e.g., non-infected tissue vs. a infected tissue).
  • a reference sample can also be from an untreated donor or cell culture not treated with an active agent (e.g., no treatment or administration of vehicle only).
  • a reference sample can also be taken at a "zero time point" prior to contacting the cell or subject with the agent to be tested.
  • Similarity or “percent similarity” in the context of two or more polypeptide sequences, refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues, or conservative substitutions thereof, that are the same when compared and aligned for maximum correspondence, as measured using one of the following sequence comparison algorithms, or by visual inspection.
  • stable or “stabilized”, as used herein with reference to a polypeptide, refers to polypeptides which have been hydrocarbon-stapled to promote and/or maintain helical structure and/or improve protease resistance and/or improve acid stability and/or improve thermal stability and/or improve pharmacologic properties. Stabilized polypeptides are a type of structurally constrained polypeptides.
  • structurally constrained peptides and the like are understood to include modified peptides having any (i.e., at least one) chemical modification, e.g., mutation of the original or native sequence with a natural or non-natural amino acid; chemical modification to incorporate a molecular tether; chemical modification to promote the formation of a disulfide bridge; etc. such that the structurally constrained peptide adopts a more limited number of structures than the unmodified peptide.
  • a structurally constrained peptide can include 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or more mutations as compared to the native, wild-type sequence.
  • molecular tethers can include hydrocarbon staples to promote the formation of stable helical structures, especially alpha-helical and 3io structures, or kinks depending on the positions of the ends of the tethers and the lengths of the tethers.
  • Natural or non- natural amino acids can be employed to promote kinks (e.g., bends in the structure as defined by the variable angles between the two adjoining structures) or other preferred confirmations.
  • the natural amino acid proline can induce a kink in a peptide due to the structure of the amino acid R group and the lack of a hydrogen- bond donor.
  • Non-natural amino acids particularly those having large and/or charged R groups, or N-methylated amides, N-substituted glycines, cyclic alpha.alpha- disubstitution, cyclic ⁇ , ⁇ -disubstitution, and beta-amino acids can promote specific, desired confirmations. It is understood that a population of "structurally constrained" peptides in solution may not all have the desired confirmation all of the time. Instead, in a population of structurally constrained peptides in solution, the desired confirmation is present at least about 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or more of the time than the native or original peptide sequence in solution prior to chemical modification.
  • the structure of a population of peptides in solution can be determined by various methods known to those of skill in the art including, but not limited to, circular dichroism and NMR spectroscopy. Xray crystallography can be applied to determine the structure of a constrained peptide when packed in the form of a crystal.
  • Small molecule as used herein is understood as a compound, typically an organic compound, having a molecular weight of no more than about 1500 Da, 1000 Da, 750 Da, or 500 Da. In an embodiment, a small molecule does not include a polypeptide or nucleic acid including only natural amino acids and/or nucleotides.
  • An agent, polypeptide, nucleic acid, or other compound "specifically binds" a target molecule, e.g., antigen, polypeptide, nucleic acid, or other compound, when the target molecule is bound with at least 100-fold, preferably at least 500-fold, preferably at least 1000-fold, preferably at least a 5000-fold, preferably at least a 10,000-fold preference as compared to a non-specific compounds, or a pool of non-specific compounds.
  • binds can be used in relation to binding one of two or more related compounds that have physically related structures. Binding preferences and affinities, absolute or relative, can be determined, for example by determining the affinity for each pair separately or by the use of competition assays or other methods well known to those of skill in the art.
  • a "subject” as used herein refers to living organisms.
  • the living organism is an animal.
  • the subject is a mammal.
  • the subject is a domesticated mammal. Examples of subjects include humans, monkeys, dogs, cats, mice, rats, cows, horses, goats, and sheep.
  • a human subject may also be referred to as a patient.
  • a subject "suffering from or suspected of suffering from” a specific disease, condition, or syndrome has a sufficient number of risk factors or presents with a sufficient number or combination of signs or symptoms of the disease, condition, or syndrome such that a competent individual would diagnose or suspect that the subject was suffering from the disease, condition, or syndrome.
  • “Therapeutically effective amount,” as used herein refers to an amount of an agent which is effective, upon single or multiple dose administration to the cell or subject, in prolonging the survivability of the patient with such a disorder, reducing one or more signs or symptoms of the disorder, preventing or delaying infection, preventing or delaying the progression of a disease or disorder and the like beyond that expected in the absence of such treatment.
  • An agent can be administered to a subject, either alone or in combination with one or more therapeutic agents, as a pharmaceutical composition in mixture with conventional excipient, e.g., pharmaceutically acceptable carrier, or therapeutic treatments.
  • the pharmaceutical agents may be conveniently administered in unit dosage form and may be prepared by any of the methods well known in the pharmaceutical arts, e.g., as described in Remington's Pharmaceutical Sciences (Mack Pub. Co., Easton, PA, 1985).
  • Formulations for parenteral administration may contain as common excipients such as sterile water or saline, polyalkylene glycols such as polyethylene glycol, oils of vegetable origin, hydrogenated naphthalenes and the like.
  • biocompatible, biodegradable lactide polymer, lactide/glycolide copolymer, or polyoxyethylene-polyoxypropylene copolymers may be useful excipients to control the release of certain agents.
  • active compounds used in a given therapy will vary according to e.g., the specific compound being utilized, the particular composition formulated, the mode of administration and characteristics of the subject, e.g., the species, sex, weight, general health and age of the subject.
  • Optimal administration rates for a given protocol of administration can be readily ascertained by those skilled in the art using conventional dosage determination tests conducted with regard to the foregoing guidelines.
  • susceptible to or “prone to” or “predisposed to” a specific disease or condition and the like refers to an individual who based on genetic, environmental, health, and/or other risk factors is more likely to develop a disease or condition than the general population.
  • An increase in likelihood of developing a disease may be an increase of about 10%, 20%, 50%, 100%, 150%, 200%, or more.
  • alkyl refers to a hydrocarbon chain that may be a straight chain or branched chain, containing the indicated number of carbon atoms.
  • Cr Cio indicates that the group may have from 1 to 10 (inclusive) carbon atoms in it.
  • alkyl is a chain (straight or branched) having 1 to 20 (inclusive, i.e., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20) carbon atoms in it.
  • alkylene refers to a divalent alkyl (i.e.,— R ⁇ ).
  • alkenyl refers to a hydrocarbon chain that may be a straight chain or branched chain having one or more carbon-carbon double bonds.
  • the alkenyl moiety contains the indicated number of carbon atoms. For example, C 2 -Cio indicates that the group may have from 2 to 10 (inclusive) carbon atoms in it.
  • lower alkenyl refers to a C 2 -C 8 alkenyl chain. In the absence of any numerical designation, "alkenyl” is a chain (straight or branched) having 2 to 20 (inclusive) carbon atoms in it.
  • alkynyl refers to a hydrocarbon chain that may be a straight chain or branched chain having one or more carbon-carbon triple bonds.
  • the alkynyl moiety contains the indicated number of carbon atoms. For example, C 2 -Ci 0 indicates that the group may have from 2 to 10 (inclusive) carbon atoms in it.
  • lower alkynyl refers to a C 2 -C 8 alkynyl chain. In the absence of any numerical designation, “alkynyl” is a chain (straight or branched) having 2 to 20 (inclusive) carbon atoms in it.
  • aryl refers to a 6-carbon monocyclic or 10-carbon bicyclic aromatic ring system wherein 0, 1, 2, 3, or 4 atoms of each ring may be substituted by a substituent. Examples of aryl groups include phenyl, naphthyl and the like.
  • arylalkyl or the term “aralkyl” refers to alkyl substituted with an aryl.
  • arylalkoxy refers to an alkoxy substituted with aryl.
  • cycloalkyl as employed herein includes saturated and partially unsaturated cyclic hydrocarbon groups having 3 to 12 carbons, preferably 3 to 8 carbons, and more preferably 3 to 6 carbons, wherein the cycloalkyl group additionally may be optionally substituted.
  • Preferred cycloalkyl groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl.
  • halo refers to any radical of fluorine, chlorine, bromine or iodine.
  • heteroaryl refers to an aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2, 3, or 4 atoms of each ring may be substituted by a substituent.
  • heteroaryl groups include pyridyl, furyl or furanyl, imidazolyl, benzimidazolyl, pyrimidinyl, thiophenyl or thienyl, quinolinyl, indolyl, thiazolyl, and the like.
  • heteroarylalkyl or the term “heteroaralkyl” refers to an alkyl substituted with a heteroaryl.
  • heteroarylalkoxy refers to an alkoxy substituted with heteroaryl.
  • heterocyclyl refers to a nonaromatic 5-8 membered monocyclic, 8- 12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2 or 3 atoms of each ring may be substituted by a substituent.
  • heterocyclyl groups include piperazinyl, pyrrolidinyl, dioxanyl, morpholinyl, tetrahydrofuranyl, and the like.
  • substituted refers to a group “substituted” on an alkyl, cycloalkyl, aryl, heterocyclyl, or heteroaryl group at any atom of that group.
  • Suitable substituents include, without limitation, halo, hydroxy, mercapto, oxo, nitro, haloalkyl, alkyl, alkaryl, aryl, aralkyl, alkoxy, fhioalkoxy, aryloxy, amino, alkoxycarbonyl, amido, carboxy, alkanesulfonyl, alkylcarbonyl, and cyano groups.
  • Ranges provided herein are understood to be shorthand for all of the values within the range. This includes all individual sequences when a range of SEQ ID NOs: is provided.
  • a range of 1 to 50 is understood to include any number, combination of numbers, or sub-range from the group consisting 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50.
  • the term "about” is understood as within a range of normal tolerance in the art, for example within 2 standard deviations of the mean. About can be understood as within 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05%, or 0.01% of the stated value. Unless otherwise clear from context, all numerical values provided herein can be modified by the term about.
  • compositions or methods provided herein can be combined with one or more of any of the other compositions and methods provided herein.
  • Pharmaceutical compositions and routes of administration can be combined with one or more of any of the other compositions and methods provided herein.
  • One or more structurally constrained peptide of the instant invention can be used in a pharmaceutical composition for the treatment of a disorder provided herein.
  • Treatment method provided herein can be performed using a combination of the structurally constrained peptides, which can be selected and combined to treat the disorder in the subject.
  • a pharmaceutical composition of the instant invention can include 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or more structurally constrained peptides.
  • the structurally constrained peptides can also be combined with other agents, e.g., anti-cancer agents or angiogenesis inhibitors.
  • the compounds of this invention are defined to include pharmaceutically acceptable derivatives thereof.
  • a "pharmaceutically acceptable derivative” means any pharmaceutically acceptable salt, ester, salt of an ester, or other derivative of a compound of this invention which, upon administration to a recipient, is capable of providing (directly or indirectly) a compound of this invention.
  • Particularly favored derivatives are those that increase the bioavailability of the compounds of this invention when such compounds are administered to a mammal (e.g., by allowing an orally administered compound to be more readily absorbed into the blood, to increase serum stability or decrease clearance rate of the compound) or which enhance delivery of the parent compound to a biological compartment (e.g., the brain or lymphatic system) relative to the parent species.
  • Derivatives include derivatives where a group which enhances aqueous solubility or active transport through the gut membrane is appended to the structure of formulae described herein.
  • the compounds of this invention may be modified by appending appropriate functionalities to enhance selective biological properties. Such modifications are known in the art and include those which increase biological penetration into a given biological compartment (e.g., blood, lymphatic system, central nervous system), increase oral availability, increase solubility to allow administration by injection, alter metabolism and alter rate of excretion.
  • Pharmaceutically acceptable salts of the compounds of this invention include those derived from pharmaceutically acceptable inorganic and organic acids and bases.
  • Suitable acid salts include acetate, adipate, benzoate, benzenesulfonate, butyrate, citrate, digluconate, dodecylsulfate, formate, fumarate, glycolate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, lactate, maleate, malonate, methanesulfonate, 2- naphthalenesulfonate, nicotinate, nitrate, palmoate, phosphate, picrate, pivalate, propionate, salicylate, succinate, sulfate, tartrate, tosylate and undecanoate.
  • Salts derived from appropriate bases include alkali metal (e.g., sodium), alkaline earth metal (e.g., magnesium), ammonium and N-(alkyl)4+ salts.
  • alkali metal e.g., sodium
  • alkaline earth metal e.g., magnesium
  • ammonium e.g., sodium
  • N-(alkyl)4+ salts e.g., sodium
  • This invention also envisions the quaternization of any basic nitrogen-containing groups of the compounds disclosed herein. Water or oil-soluble or dispersible products may be obtained by such quaternization.
  • the compounds of the invention can, for example, be administered by injection, intravenously, intraarterially, subdermally, intraperitoneally, intramuscularly, or subcutaneously; or orally, buccally, nasally, transmucosally, intravaginally, cervically, topically, in an ophthalmic preparation, or by inhalation, with a dosage ranging from about 0.001 to about 100 mg/kg of body weight, or according to the requirements of the particular drug and more preferably from 0.5- lOmg/kg of body weight.
  • the methods herein contemplate administration of an effective amount of compound or compound composition to achieve the desired or stated effect.
  • the amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
  • a typical preparation will contain from about 1% to about 95% active compound (w/w).
  • such preparations contain from about 20% to about 80% active compound.
  • compositions of this invention comprise compounds of the invention or a pharmaceutically acceptable salt thereof; an additional agent including for example, one or more therapeutic agents for the prevention and/or treatment of a disorder provided herein, particularly for the prevention and/or treatment of cancer, and any pharmaceutically acceptable carrier, adjuvant or vehicle.
  • compositions of this invention comprise a compound of the invention or a pharmaceutically acceptable salt thereof; and a pharmaceutically acceptable carrier, adjuvant or vehicle.
  • compositions delineated herein include the compounds of the invention delineated herein, as well as additional therapeutic agents if present, in amounts effective for achieving a modulation of disease or disease symptoms, including cancer or symptoms thereof.
  • pharmaceutically acceptable carrier or adjuvant refers to a carrier or adjuvant that may be administered to a patient, together with a compound of this invention, and which does not destroy the pharmacological activity thereof and is nontoxic when administered in doses sufficient to deliver a therapeutic amount of the compound.
  • Pharmaceutically acceptable earners, adjuvants and vehicles that may be used in the pharmaceutical compositions of this invention include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d-a.-tocopherol polyethyleneglycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tween® or other similar polymeric delivery matrices, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, poly
  • Cyclodextrins such as alpha-, beta-, and gamma-cyclodextrin, may also be advantageously used to enhance delivery of compounds of the formulae described herein.
  • the pharmaceutical compositions of this invention may be administered enterally for example by oral administration, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir, preferably by oral or vaginal administration or administration by injection.
  • the pharmaceutical compositions of this invention may contain any conventional nontoxic pharmaceutically-acceptable carriers, adjuvants or vehicles.
  • the pH of the formulation may be adjusted with pharmaceutically acceptable acids, bases, or buffers to enhance the stability of the formulated compound or its delivery form.
  • parenteral as used herein includes subcutaneous, intracutaneous, intravenous, intramuscular, intraarticular, intraarterial, intrasynovial, intrastemal, intrathecal, intralesional, and intracranial injection or infusion techniques.
  • dosage forms include, but are not limited to: tablets; caplets; capsules, such as soft elastic gelatin capsules; cachets; troches; lozenges; dispersions; suppositories; ointments; cataplasms (poultices); pastes; powders; dressings; creams; plasters; solutions; patches; aerosols (e.g., nasal sprays or inhalers); gels; liquid dosage forms suitable for oral or mucosal administration to a patient, including suspensions (e.g., aqueous or non-aqueous liquid suspensions, oil-in-water emulsions, or a water-in-oil liquid emulsions), solutions, and elixirs; liquid dosage forms suitable for parenteral administration to a patient; and sterile solids (e.g., crystalline or amorphous solids) that can be reconstituted to provide liquid dosage forms suitable for parenteral administration to a patient.
  • suspensions e.g., aqueous
  • the pharmaceutical compositions may be in the form of a sterile injectable preparation, for example, as a sterile injectable aqueous or oleaginous suspension.
  • This suspension may be formulated according to techniques known in the art using suitable dispersing or wetting agents (such as, for example, Tween® 80) and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol.
  • suitable vehicles and solvents that may be employed are mannitol, water, Ringer's solution and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil may be employed including synthetic mono- or diglycerides.
  • Fatty acids, such as oleic acid and its glyceride derivatives are useful in the preparation of injectables, as are natural pharmaceutically-acceptable oils, such as olive oil or castor oil, especially in their polyoxyethylated versions.
  • These oil solutions or suspensions may also contain a long-chain alcohol diluent or dispersant, or carboxymethyl cellulose or similar dispersing agents which are commonly used in the formulation of pharmaceutically acceptable dosage forms such as emulsions and or suspensions.
  • surfactants such as Tweens or Spans and/or other similar emulsifying agents or bioavailability enhancers which are commonly used in the manufacture of pharmaceutically acceptable solid, liquid, or other dosage forms may also be used for the purposes of formulation.
  • compositions of this invention may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, emulsions and aqueous suspensions, dispersions and solutions.
  • carriers which are commonly used include lactose and corn starch.
  • Lubricating agents such as magnesium stearate, are also typically added.
  • useful diluents include lactose and dried corn starch.
  • aqueous suspensions and/or emulsions are administered orally, the active ingredient may be suspended or dissolved in an oily phase and is combined with emulsifying and/or suspending agents. If desired, certain sweetening and/or flavoring and/or coloring agents may be added.
  • compositions of this invention may also be administered in the form of suppositories for rectal administration.
  • These compositions can be prepared by mixing a compound of this invention with a suitable non-irritating excipient which is solid at room temperature but liquid at the rectal temperature and therefore will melt in the rectum to release the active components.
  • suitable non-irritating excipient include, but are not limited to, cocoa butter, beeswax and polyethylene glycols.
  • the pharmaceutical compositions of the invention may be administered topically or intravaginally.
  • the pharmaceutical composition will be formulated with a suitable ointment containing the active components suspended or dissolved in a carrier.
  • Carriers for topical administration of the compounds of this invention include, but are not limited to, mineral oil, liquid petroleum, white petroleum, propylene glycol, polyoxyethylene polyoxypropylene compound, emulsifying wax and water.
  • the pharmaceutical composition can be formulated with a suitable lotion or cream containing the active compound suspended or dissolved in a carrier.
  • the pharmaceutical composition is formulated as a vaginal ring.
  • Suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water.
  • the pharmaceutical compositions of this invention may also be topically applied to the lower intestinal tract by rectal suppository formulation or in a suitable enema formulation. Topically-transdermal patches and iontophoretic administration are also included in this invention.
  • compositions of this invention may be administered by nasal aerosol or inhalation.
  • Such compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other solubilizing or dispersing agents known in the art.
  • compositions of this invention comprise a combination of a compound of the formulae described herein and one or more additional therapeutic or prophylactic agents
  • both the compound and the additional agent should be present at dosage levels of between about 1 to 100%, and more preferably between about 5 to 95% of the dosage normally administered in a monotherapy regimen.
  • the additional agents may be administered separately, as part of a multiple dose regimen, from the compounds of this invention. Alternatively, those agents may be part of a single dosage form, mixed together with the compounds of this invention in a single composition.
  • Effective dosages of the peptides of the invention to be administered may be determined through procedures well known to those in the art which address such parameters as biological half -life, bioavailability, and toxicity.
  • a therapeutically effective dose refers to that amount of the compound sufficient to result in amelioration of symptoms or a prolongation of survival in a patient.
  • Toxicity and therapeutic efficacy of such compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., for determining the LD 50 (the dose lethal to 50% of the population) and the ED 50 (the dose therapeutically effective in 50% of the population).
  • the dose ratio between toxic and therapeutic effects is the therapeutic index and it can be expressed as the ratio LD50/ED50.
  • Compounds which exhibit large therapeutic indices are preferred. The data obtained from these cell culture assays and animal studies can be used in formulating a range of dosage for use in humans.
  • the dosage of such compounds lies preferably within a range of circulating concentrations that include the ED50 with little or no toxicity.
  • the dosage may vary within this range depending upon the dosage form employed and the route of administration utilized.
  • the therapeutically effective dose can be estimated initially from cell culture assays.
  • a dose may be formulated in animal models to achieve a circulating plasma concentration range that includes the IC50 (e.g., the concentration of the test compound which achieves a half-maximal inhibition of the BCL9/b-catenin protein interaction or functional surrogate thereof as measured by an assay relative to the amount of the event in the absence of the test compound) as determined in cell culture.
  • IC50 e.g., the concentration of the test compound which achieves a half-maximal inhibition of the BCL9/b-catenin protein interaction or functional surrogate thereof as measured by an assay relative to the amount of the event in the absence of the test compound
  • levels in plasma may be measured, for example, by high performance liquid chromatography (HPLC
  • the present invention also encompasses a finished packaged and labeled pharmaceutical product or laboratory reagent.
  • This article of manufacture includes the appropriate instructions for use in an appropriate vessel or container such as a glass vial or other container that is hermetically sealed.
  • a pharmaceutical product may contain, for example, a compound of the invention in a unit dosage form in a first container, and in a second container, sterile water or adjuvant for injection.
  • the unit dosage form may be a solid suitable for oral, transdermal, intranasal, intravaginal, cervical ring, or topical delivery.
  • the unit dosage form is suitable for intravenous, intramuscular, intraperitoneal, intranasal, oral, intravaginal, cervical, topical or subcutaneous delivery.
  • the invention encompasses solutions, solids, foams, gels, preferably sterile, suitable for each delivery route.
  • the packaging material and container are designed to protect the stability of the product during storage and shipment.
  • the products of the invention include instructions for use or other informational material that advise the physician, technician, or patient on how to appropriately prevent or treat the disease or disorder in question.
  • the article of manufacture includes instructions indicating or suggesting a dosing regimen including, but not limited to, actual doses, monitoring procedures (e.g., detection and quantitation of infection), and other monitoring information.
  • the invention provides an article of manufacture including packaging material, such as a box, bottle, tube, vial, container, sprayer, insufflator, intravenous (i.v.) bag, envelope and the like; and at least one unit dosage form of a pharmaceutical agent contained within said packaging material, wherein said pharmaceutical agent comprises a compound of the invention, and wherein said packaging material includes instruction means which indicate that said compound can be used to manage, treat, and/or ameliorate one or more symptoms associated with a disease provided herein, by administering specific doses and using specific dosing regimens as described herein.
  • packaging material such as a box, bottle, tube, vial, container, sprayer, insufflator, intravenous (i.v.) bag, envelope and the like
  • said packaging material includes instruction means which indicate that said compound can be used to manage, treat, and/or ameliorate one or more symptoms associated with a disease provided herein, by administering specific doses and using specific dosing regimens as described herein.
  • the disease or disorder treated by the stabilized peptides of the invention is associated with angiogenesis.
  • the disease is selected from: tumor or cancer growth (neoplasia), skin disorders, neovascularization, inflammatory and arthritic diseases, retinoblastoma, cystoid macular edema (CME), exudative age-related macular degeneration (AMD), diabetic retinopathy, diabetic macular edema, or ocular inflammatory disorders.
  • the structurally constrained peptides of the invention can be used for overcoming cancer stem cell chemo- and radioresistance (treatment- resistance).
  • the disease or disorder is tumor or cancer growth (neoplasia).
  • the disease or disorder is ocular cancer, rectal cancer, colon cancer, colorectal caner, cervical cancer, prostate cancer, breast cancer, bladder cancer, oral cancer, benign and malignant tumors, stomach cancer, liver cancer, pancreatic cancer, lung cancer, corpus uteri, ovary cancer, prostate cancer, testicular cancer, renal cancer, brain/ens cancer, throat cancer, multiple myeloma, skin melanoma, acute lymphocytic leukemia, acute myelogenous leukemia, Ewing's Sarcoma, Kaposi's Sarcoma, basal cell carinoma and squamous cell carcinoma, small cell lung cancer, choriocarcinoma, rhabdomyosarcoma, angios
  • the disease or disorder is a skin disorder.
  • the disease or disorder is psoriasis, acne, rosacea, warts, eczema, hemangiomas, lymphangiogenesis, Sturge-Weber syndrome, venous ulcers of the skin, neurofibromatosis, and tuberous sclerosis.
  • the disease or disorder is neovascularization.
  • the disease or disorder is diabetic retinopathy, retinopathy of prematurity, corneal graft rejection, neovascular glaucoma, retrolental fibroplasias, epidemic keratoconjunctivitis, vitamin A deficiency, contact lens overwear, atopic keratitis, superior limbic keratitis, pterygium keratitis sicca, Sjogren's, acne rosacea, phylectenulosis, syphilis, Mycobacteria infections, lipid degeneration, chemical burns, bacterial ulcers, fungal ulcers, herpes simplex infections, herpes zoster infections, protozoan infections, Kaposi's sarcoma, Mooren's ulcer, Terrien's marginal degeneration, marginal keratolysis, trauma, rheumatoid arthritis, systemic lupus, poly
  • the disease or disorder is inflammatory and arthritic disease.
  • the disease or disorder is rheumatoid arthritis, osteoarthritis, lupus, scleroderma, Crohn's disease, ulcerative colitis, psoriasis, sarcoidosis, Sarcoidosis, skin lesions, hemangiomas, Osier- Weber-Rendu disease, hereditary hemorrhagic telangiectasia, and osteoarthritis.
  • the disease or disorder affects the dermis, epidermis, endometrium, retina, surgical wound, gastrointestinal tract, umbilical cord, liver, kidney, reproductive system, lymphoid system, central nervous system, breast tissue, urinary tract, circulatory system, bone, muscle, or respiratory tract.
  • the standard Fmoc protocol employed 2 x 10 min deprotections in 20% piperidine/NMP followed by a pair of consecutive methanol and dimethylformamide (DMF) washes.
  • the incorporated non-natural amino acids were treated with 4 x 10 min incubations in 20% piperidine/NMP to achieve complete deprotection.
  • Amino acid coupling was performed using 0.4 M stock solutions of Fmoc-protected amino acids, 0.67 M 2-(6-chloro-lH-benzotriazole-l-yl)-l, 1,3,3- tetramethylaminium hexafluorophosphate (HCTU), and 2 M N,N-diisopropyl ethylamine (DIEA), yielding 1 mL of 0.2 M active ester (4 equivalents).
  • Coupling frequency and incubation times were 2 x 30 min for standard residues, 2 x 45 min for the olefinic non-natural amino acids, and 3 x 45 min for the residue following a non- natural amino acid.
  • the amino terminus was either acetylated or capped with Fmoc- -Ala for FITC derivatization.
  • the resin was charged with a 10 mM solution of bis(tricyclohexylphosphine)-benzylidene ruthenium (IV) dichloride (Grubbs' first generation catalyst) in 1,2-dichloroethane and stirred for 2 hours twice.
  • Fmoc- -Ala was deprotected with piperidine in NMP and then reacted with fluorescein isothiocyante (FITC) and triethylamine in dimethylformamide overnight.
  • FITC fluorescein isothiocyante
  • TFA/triisopropyl silane (TIS)Avater 95%, 2.5%, 2.5%), and precipitated with diethylether/hexanes.
  • Stapled peptides were purified by reverse- phase HPLC (Agilent) using a C18 column (Zorbax), characterized by LC MS (mass spectra obtained using electrospray in positive ion mode), and quantified by amino acid analysis (AAA) on a Beckman 6300 high-performance amino acid analyzer.
  • Working stock solutions were generated by dissolving the lyophilized powder in 100% DMSO at 1 to 10 mM.
  • SAH-gp41 powder and DMSO solutions were stored at -20°C. Determination of -helicity was performed as previously described (Walensky, L. D. et al. Science 305, 1466-70 (2004); Bird, G. H., et al., Methods Enzymol 446, 369-86 (2008)). See experimental results in Fig. la-lc, lg.
  • Recombinant human BCL9 (214-493) was cloned into pET-23a (+)was cloned into pET-23a (+) vector (Novagen) containing carboxy- terminal hexa-histidine tag.
  • the lysates were then centrifuged and loaded onto HIS-Select Nickel Affinity Gel (Sigma) and washed with wash buffer (50 mM NaH2P04, pH 8.0, 0.3M NaCl and 10 mM imidazole).
  • wash buffer 50 mM NaH2P04, pH 8.0, 0.3M NaCl and 10 mM imidazole.
  • the protein was eluted in 50 mM Na 2 HP0 4 , pH 8.0, 0.3M NaCl and 250 mM imidazole and dialyzed overnight in sterile lx PBS.
  • Human ⁇ -catenin constructs (e.g., residues 1-781, 138-683, 273- 684) were cloned into pGEX4Tl/pGEX4T2, pET-28a, and pET-23a respectively.
  • His-tagged fusion proteins were generated as described above for BCL9.
  • transformed E. coli BL21 (DE3) were cultured at 37°C to A600 - 0.6 and induced with 1 mM IPTG for 4 h. Cells were pelleted, resuspended and sonicated in Buffer A (50 mM Tris, pH 8.0, 150 MM NaCl, sucrose 20%, 5 mM dithiothreitol (DTT), ImM EDTA, 1 mM PMSF, 2 mg/ml aprotinin, and 0.7 mg/ml pepstatin).
  • Buffer A 50 mM Tris, pH 8.0, 150 MM NaCl, sucrose 20%, 5 mM dithiothreitol (DTT), ImM EDTA, 1 mM PMSF, 2 mg/ml aprotinin, and 0.7 mg/ml pepstatin).
  • Solubilized proteins were adsorbed to glutathione-Sepharose 4B beads (GE), which were then eluted in Buffer A with 20 mM gluthatione and dialyzed against PBS buffer supplemented with protease inhibitor cocktail tablets (Roche).
  • GE glutathione-Sepharose 4B beads
  • Equal amounts (0.5 ⁇ ) of His-tagged BCL9 and GST-tagged ⁇ -catenin bound to glutathione-Sepharose 4B beads (GE) were incubated with or without increasing amounts of HD2 or SAH-BCL9 peptides for 1 h at 4°C in a final volume of 1000 ⁇ PBS. Protein complexes were pelleted by centrifugation at 2000 rpm for 2 min and beads washed four times with PBS buffer. The beads were then taken up in SDS- PAGE loading buffer, boiled, and SDS-PAGE performed to visualize bound proteins by Coomassie staining.
  • Example 4 Patient samples and cell lines Bone marrow specimens were obtained from patients with MM in accordance with Dana-Farber Cancer Institute Review Board approval and informed consent performed in compliance with the Declaration of Helsinki. Primary CD 138+ plasma cells were purified using magnetic beads as described (Sukhdeo, K. et al. Proc Natl Acad Sci U S A 104, 7516-21 (2007)). CRC primary tumor samples were obtained from the Brigham and Women's Hospital in accordance with the policies of their Institutional Review Board. To generate sufficient CRC primary tumor cells for experimentation, the primary tumors were first expanded subcutaneously in NOD/SCID mice (Jackson Laboratory).
  • mice were sacrificed according to institutional guidelines and subcutaneous tumor xenografts were minced with a scalpel and digested by incubation with collagenase IV (Worthington Biomedical Corporation) and 0.01 % DNase I (Sigma-Aldrich) at 37°C for 30 min, followed by additional mechanical disaggregation using a Stomacher device (Seward Laboratory Systems Inc.). Samples were filtered through a 70 ⁇ cell strainer and washed with PBS. Red blood cells were lysed using ACK lysing buffer (BioWhittaker, Lonza) and viable tumor cells were enriched by Ficoll-Paque gradient centrifugation (GE Healthcare).
  • BCL9 (ab37305, Abeam), B9L (AF4967, R&D Systems), ⁇ -catenin (CAT5-H10, Zymed), FITC (abl9224, Abeam), Actin-HRP (C-l l, Santa Cruz), Caspase3 (#9662, Cell Signaling), ⁇ (#9242, Cell signaling), PARP (#9542, Cell Signaling), E-cadherin (#3195, Cell Signaling), and Lamin B (sc-6217, Santa Cruz).
  • Horseradish peroxidase conjugated secondary antibodies were purchased from Santa Cruz and SouthernBiotech. Co- immunoprecipitation was performed as described (Walensky, L. D.
  • Example 6 SAH-BCL9 cellular uptake and localization analyses
  • cells were prepared using a cytocentrifuge (Thermo Shandon) and fixed as previously described (Sukhdeo, K. et al. Proc Natl Acad Sci U S A 104, 7516-21 (2007); Mani, M. et al. Cancer Res 69, 7577-86 (2009)).
  • Anti- -catenin and rhodamine-conjugated secondary antibodies (5 ⁇ g/ml; Southern Biotechnology) were employed. Images were obtained using a BioRad Radiance 2000 laser scanning confocal microscope.
  • Cell permeability of SAH-BCL9B and SAH-BCL9 fl were determined by fluorescence microscopy of cells treated with FITC-derivatives of the above described stapled peptides and also by blotting/fluorescence scan, performed as previously described (Pitter, K. et al Methods Enzymol, 446, (2008), 387-408; Walensky, L. D. et al. Science 305, 1466-70 (2004). See results in Fig. le, 7.
  • Tissue sections were process as described (Sukhdeo, K. et al. Proc Natl Acad Sci U S A 104, 7516-21 (2007)). Sections were incubated with primary antibodies (5 ⁇ g/ml) or the corresponding IgG fraction of preimmune serum overnight at 4°C in blocking solution (3 % BSA/PBS). BCL9 (ab37305, Abeam), mouse CD34 (RAM34, eBiosciences), human CD34 (M7165, Dako) and human CD44H (2C5, R&D Systems) antibodies were employed.
  • Blood vessel formation in the CRC and MM models was evaluated using anti-mouse CD34 and anti-human CD34 antibodies, respectively, and the corresponding biotinylated antibodies coupled to streptavidin peroxidase (Vector).
  • the number of blood vessels was determined by counting the mean number of independent blood vessels in 5 randomly selected fields at 50 x magnification as highlighted by CD34 staining (brown color). See results in Fig. 4b, 4e, 4i, 6.
  • RNA from SAH-BCL9 B and vehicle (0.1 % DMSO)-treated cells were run on an Affymetrix U133A 2.0 array chip as described (Mollering et al, Nature 462, 182-8 (2009). Statistical analyses were performed in R (http://www.r-project.org). The array data were normalized with rma method (Bolstad, B. M., et al.. Bioinformatics 19, 185-93 (2003)) as implemented in the Affy package
  • Example 10 Cell proliferation, viability assay and detection of apoptosis
  • Cell proliferation assays were performed as described (Sukhdeo, K. et al. Proc Natl Acad Sci U S A 104, 7516-21 (2007)). Cell viability was measured using the CellTiter-Glo assay (Promega) according to the manufacturer's instructions. Apoptosis was evaluated by activated caspase-3 and PARP western blotting. See results in Figs. 3a-f, 13, and 20.
  • HUVEC was cultured on polymerized matrix gel and exposed to supernatant media collected from Colo320 or MM IS cells treated with vehicle (0.5 % DMSO), SAH-BCL9 B peptides (5 ⁇ ) for 24 h.
  • vehicle 0.5 % DMSO
  • SAH-BCL9 B peptides 5 ⁇
  • the number of capillary tubes formed after 5 h treatment at 37°C was determined by counting 5 randomly selected fields at 40 x magnification, according to manufacture's instructions.
  • HUVEC cultured in VEGF media and VEGF-free media were used as positive and negative controls, respectively.
  • vehicle 2.5 % DMSO in D5W
  • SAH-BCL9 peptides 20 mg/kg
  • mice Forty days after tumor cell injection, the mice were euthanized and GFP-positive tumor visualized using an ImageQuant LAS-4000 (GE Healthcare). Complete necropsies were performed for each experimental animal and livers were sectioned in their entirety at 5 mm intervals for quantitation of tumor metastases. Tissues were subjected to H&E staining and immunohistochemical analysis using anti-CD34 and anti-CD44 antibodies.
  • mice For the SCID-hu murine model of human MM, human fetal bone grafts measuring 1.5 x 0.5 cm were subcutaneously implanted into eight week old male CB-17 SCID mice (Taconic) as previously described (Tassone, P. et al. Blood 106, 713-6 (2005)). Four weeks after bone implantation, 5 x 10 6 GFP-positive ⁇ -6 MM cells were injected directly into each bone implant. Two days later, mice were treated with 100 ⁇ injections of vehicle (2.5 % DMSO in D5W) or SAH-BCL9 peptides (5 mg/kg) instilled adjacent to the bone chips on alternate days for a total of 10 doses.
  • vehicle 2.5 % DMSO in D5W
  • SAH-BCL9 peptides 5 mg/kg
  • mice were sacrificed and analyzed for tumor burden by fluorescence imaging and histologic analysis of the bone grafts. See results in Figs. 4a-i.
  • TUNEL staining was performed on samples obtained from the mice. The results demonstrated that there is an increase in apoptotic tumor cells in animals treated with SAH-BCL9B compared to vehicle or SAH-BCL9 A i £/ r- treated mice. See results in Figs. 22 and 23. All animal experiments were performed in accordance with approved protocols of the Dana-Farber Cancer Institute Animal Care and Use Committee. Example 13. In vivo effect of SAH-BCL9 B on Wnt reporter activity
  • HCT116 cells were transfected with pOT-Luc plasmid or a control UbC-Luc plasmid.
  • the pOT-Luc reporter activity was normalized to UbC-Luc activity. See results in Fig. 9.
  • VEGF ELISA was performed as previously described (Mani, M. et al. Cancer Res 69, 7577-86 (2009)). Briefly, cells (lxlO 6 ) were treated with vehicle and SAH-BCL9 peptides (5 ⁇ ) for 24 h. VEGF levels in the supernatant were then measured according to the manufacturer's ELISA protocol (DuoSet, R&D Systems).
  • Example 15 Chromatin immunoprecipitation (ChIP) and polymerase chain reaction (PCR) Antibody (3 ⁇ g) was prebound for 8 h to protein A and protein G Dynal magnetic beads (Dynal Biotech, Norway) and washed 5 times with ice-cold PBS containing 5 % BSA, and then added to the diluted chromatin for overnight immunoprecipitation using the following antibodies: TCF-4 (Upstate #05-511), mouse IgG2a isotype control (Sigma, M5409), and rabbit IgG (sc-2027, Santa Cruz).
  • ChIP Chromatin immunoprecipitation
  • PCR polymerase chain reaction
  • the magnetic bead- chromatin complexes were collected and washed 6x in RIPA buffer (50 mM HEPES [pH 7.6], 1 mM EDTA, 0.7 % Na deoxycholate, 1 % NP-40, 0.5 M LiCl). DNA was eluted from the beads as previously described (Clevers, H. Cell 127, 469-80 (2006)).
  • Amplification was carried out with a PTC-200 programmable thermal controller (MJ Research) after an initial denaturation at 94°C for 5 min, followed by 30 cycles of PCR using the following temperature and time profile: denaturation at 94 °C for 0.5 min, primer annealing at 59°C for 0.5 min, primer extension at 72°C for 0.5 min, and a final extension of 72°C for 10 min.
  • the PCR products were visualized by 2 % gel electrophoresis.
  • VEGF F (Forward): 5'- gcgtgtctctggacagagttt -3' and R (Reverse): 5'- agcctcagcccttccaca-3';
  • VEGF upstream F: 5'- gaggctatgccagctgtagg -3' and R: 5'- cccttttcctccaactctcc - 3';
  • c-Myc F: 5'- actcccccggctcggtccacaagc -3', and R: 5'- cccaatttctcagccaggtttcag -3' (Klaus, A. & Birchmeier, W. Nat Rev Cancer 8, 387-98 (2008)). See results in Fig. 11a.
  • VEGF promoter luciferase assays The VEGF promoter-driven luciferase constructs (2.6-kb) were a kind gift from Soumitro Pal (Transplantation Research Center, Children's Hospital Boston and Brigham and Women's Hospital) (Basu, A. et al. Cancer Res 68, 5689-98 (2008)). Cells were transfected with the VEGF luciferase constructs using FuGENE transfection reagent (Roche) and luciferase activity was measured using Dual Luciferase Reporter Assay System (Promega) as previously described (Sukhdeo, K. et al. Proc Natl Acad Sci U S A 104, 7516-21 (2007)). See results in Fig. 1 lb.
  • a lentiviral reporter vector containing seven TCF/LEF-1 binding motifs and a minimal promoter driving destabilized GFP expression (7xTdG) was derived from the lentiviral vector TOP-dGFP, which contains three TCF/LEF-1 binding motifs (Sukhdeo, K. et al. Proc Natl Acad Sci U S A 104, 7516-21 (2007)).
  • Two synthetic complementary oligonucleotides (IDT-DNA) with four TCF/LEF-1 binding motifs (GATCAAAGG) were designed to generate compatible overhanging ends for annealing to an Xbal restriction site.
  • the oligonucleotides were annealed by heating to 95°C and slow cooling to room temperature, followed by ligating into the Xbal- linearized TOP-dGFP vector, yielding 7xTdG.
  • the 7xTOP cassette was removed from the 7xTdG vector by restriction digesting with Xmal and Agel.
  • a synthetic cassette carrying seven FOP sites (GGCCAAAGG) but otherwise identical to the removed 7xTOP cassette was inserted, yielding 7xFdG.
  • BCL9 shRNA and control shRNA lentiviral vectors were generated as reported (Sampietro, J. et al. Mol Cell 24, 293-300 (2006)). See results in Fig. 10, l ib.
  • Example 18 Lentivirus production and infection
  • HEK293T cells were plated in 10 cm tissue culture dishes and co-transfected with 10 ⁇ g lentiviral vector (either 7xTdG or 7xFdG), 10 ⁇ g pCMV-dR8.91 and 2 ⁇ g pMD2.G (Naldini et al, PNAS, 1996) using 60 ⁇ . LipoD293 (Signagen) according to the manufacturer's protocol. The media was replaced after 12 h with 30 % FCS containing DMEM (Gibco) and conditioned for 36 h.
  • Conditioned medium was then filtered through 0.45 ⁇ syringe filters (Millipore), mixed 1: 1 with fresh DMEM, and then directly used for infection of cultured Colo320 (ATCC) cells.
  • Polybrene Sigma
  • Lentivirus shRNA infections to knockdown BCL9 expression were performed as described previously (Logan, C. Y. & Nusse, R. Annu Rev Cell Dev Biol 20, 781-810 (2004)). Briefly, recombinant BCL9 shRNA and control lentiviruses were produced by transient transfection of 293T cells. Colo320 were transduced with virus supernatant containing polybrene, and GFP-expressing cells sorted by FACS. See results in Fig. 10, l ib.
  • Colo320 cells were subjected to infection for 72 h with either 7xTdG or 7xFdG lentivirus, and the transduced and control non-transduced cells were trypsinized, washed, and then analyzed on a FACSaria flow sorter. Hoechst 33258 staining was used to exclude dead cells. Single GFP-positive Colo320-7xTdG cells were sorted into 96 well plates using stringent gating on forward/side scatter height and width to exclude doublets. The presence of a single cell per well was confirmed microscopically after sorting and then single cell cultures were expanded for subsequent use. See results in Fig. l ib. Example 20. Chromatin immunoprecipitation
  • DNA was eluted from the beads as previously described (Shang, Y., et al. Cell 103, 843-52 (2000)). Amplification was carried out with a PTC-200 programmable thermal controller (MJ Research) after an initial denaturation at 94°C for 5 min, followed by 30 cycles of PCR using the following temperature and time profile: denaturation at 94 °C for 0.5 min, primer annealing at 59°C for 0.5 min, primer extension at 72°C for 0.5 min, and a final extension of 72°C for 10 min. The PCR products were visualized by 2 % gel electrophoresis.
  • VEGF B F (Forward): 5'- gcgtgtctctggacagagttt -3' and R (Reverse): 5'- agcctcagcccttccaca-3';
  • VEGF upstream F: 5'- gaggctatgccagctgtagg -3' and R: 5'- cccttttcctccaactctcc -3' ;
  • c-Myc F: 5'- actcccccggctcggtccacaagc -3' , and R: 5'- cccaatttctcagccaggtttcag -3' . See results in Fig. 11a.
  • Luciferase activity was measured using the Dual Luciferase Reporter Assay System (Promega) as previously described (Sukhdeo, K. et al. Proc Natl Acad Sci U S A 104, 7516-21 (2007)).
  • Colo320 cells were transfected with TOP-FLASH, FOP-FLASH plasmid (Millipore Corporation) or NFKB luciferase reporter (Stratagene), along with an internal Renilla control plasmid (hRL-null). Transfection was accomplished using FuGENE (Roche) according to the manufacturer's protocol. The results were normalized to control Renilla activity. The reported data represent the average of three independent transfection experiments performed in triplicate. See results in Figs. 9, 10.
  • Example 22 Selective Dissociation of the BCL9/p-catenin complex by SAH- BCL9 B
  • glutathione microtiter plates were incubated with 50 ng recombinant GST-P-catenin in 100 of ELISA buffer (PBS, 1% BSA, 0.05% Tween-20) per well and rotated (200 rpm) at 37°C for 1 hr, followed by 4- cycles of automated plate-washing with PBS, 0.05% Tween-20.
  • ELISA buffer PBS, 1% BSA, 0.05% Tween-20
  • Two-fold serial dilution of FITC-conjugated peptides in ELIS A buffer were prepared in a separate 96- well plate and transferred (100 pL) to the ⁇ -catenin-bound plate.
  • the experimental plate was incubated for 2 hr at 37°C (200 rpm), subjected to automated plate washing, and then 100 pL of a 1:7500 dilution of anti-FITC-conjugated H P in ELIS A buffer was transferred to each well for an additional 1 hr incubation at 37°C (200 rpm), followed by automated plate washing.
  • Wells were developed by adding 50 pL of tetramethylbenzidine (TMB) solution, incubating at room temperature for 20 min, and then stopping the reaction with 50 pL of 2 M H 2 S0 4 .
  • TMB tetramethylbenzidine
  • assay buffer 100 mM Na 2 P0 4 [pH7.4], 100 g/mL bovine serum albumin, 0.01% Triton X-100 and 4% DMSO.
  • FOXQ1 cgcggactttgcactttgaa; agctttaaggcacgtttgatggag
  • CDK4 atgttgtccggctgatgga; caccagggttaccttgatctcc
  • Axin2 cggaaactgttgacagtggat; ggtgcaaagacatagccagaa
  • VEGF catgaactttctgctgtcttgg; atgattctgccctcctcctttt
  • LGR5 ctcccaggtctggtgtgttg; gtgaagacgctgaggttgga
  • CMYC tttttcgggtagtggaaacc; gcagtagaaatacggctgcac
  • CD44 tttgcattgcagtcaacagtc; tgagtccacttggctttctgt
  • CLDN2 cggtgtggctaagtacaggc; caaagctcacgatggtggtct
  • LEF-1 catcccttcctcattccttcaac; aggcttcctaaaaggtggtgg
  • LGR5 was reduced in Colo320 cells but not in MM IS cells, consistent with the cellular specificity of Wnt target gene transcription.
  • SAH-BCL9B comparative genome-wide expression analyses of Wnt target genes in the DLD1 colon cancer cell line, for which a Wnt transcription pathway signature has been described (L. G. Van der Flier et al., Gastroenterology 132, 628 (2007)), was performed. RNA from triplicate SAH-BCL9 B - and vehicle-treated DLD1 samples (10 ⁇ each for 12 hours) was isolated for gene expression profiling analyses.
  • Affymetrix Human U133 Plus 2.0 arrays were processed using the function of the affy Bioconductor package (URL http://www.R-project.org.). Gene sets were compiled from Van der Flier et al. and gene set enrichment and statistical analyses performed using GSEA software (http://www.broad.mit.edu/GSEA) and a two-tailed i-test, respectively. Microarray data has been deposited in the Gene Expression Omnibus (http://www.ncbi.nlm.nih.gov/geo) and comply with MIAME annotation standards.
  • Fig. 18B family- wise error (FWER) p- value ⁇ 0.001 ; false discovery rate (FDR) q-value ⁇ 0.001) and carcinoma (Fig. 18C FWER and FDR ⁇ 0.01), highlighting the specificity of SAH-BCL9 B in blocking Wnt transcriptional activity.
  • Axin2 a robust and specific Wnt target gene(J) was among the most down-regulated genes by SAH-BCL9s treatment, in addition to other Wnt targets involved in cell metastasis ⁇ CD44, CLDN2), cell proliferation (CyclinA2, CDK4), and EMT (FOXQ1) (Figs. 18D and 18E).
  • Fig. 18F qRT-PCR
  • VEGF-A was among the genes downregulated in cells treated with SAH-BCL9 B (Figs. 18F and 19), linking the -catenin/BCL9 complex to tumor-induced angiogenesis.
  • Example 24 Combination therapies To test whether the anti-proliferative effect of SAH-BCL9s could synergize with other agents commonly used to treat MM or CRC, combination treatment studies were conducted. Indeed, the cytotoxic effects of 5-flurouracil on CRC cells and of doxorubicin on MM cells were enhanced by SAH-BCL! , but not by vehicle or the mutant peptide. See results in Fig. 21.

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Abstract

La présente invention a pour objet des peptides contraints sur le plan structural par agrafage d'hydrocarbures d'une hélice BCL9 HD2 destinés à être utilisés en tant qu'agent thérapeutique. La présente invention concerne en outre des méthodes et des kits pour l'utilisation du peptide contraint sur le plan structural selon la présente invention. La présente invention est basée, au moins en partie, sur le résultat fourni ici démontrant que des peptides hélicoïdaux à agrafage d'hydrocarbures présentent une excellente stabilité protéolytique, acide, et thermique, restaurent la structure hélicoïdale native du peptide, possèdent des propriétés pharmacocinétiques supérieures comparé aux peptides non modifiés correspondants, et sont hautement efficaces pour se lier à la β-caténine in vitro, in cellulo, et in vivo, perturber l'interaction BCL-9/β-caténine, et de ce fait interférer avec la signalisation Wnt/β-caténine dérégulée pour un bénéfice thérapeutique dans diverses maladies humaines y compris le cancer humain.
PCT/US2012/033822 2011-04-15 2012-04-16 Ciblage d'une signalisation wnt dérégulée dans le cancer à l'aide d'hélices alpha de bcl-9 stabilisées WO2012142604A2 (fr)

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EP18164082.2A EP3360892B1 (fr) 2011-04-15 2012-04-16 Ciblage de signalisation wnt déréglée du cancer utilisant des hélices alpha stabilisées de bcl-9
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US10703785B2 (en) 2020-07-07
ES2815498T3 (es) 2021-03-30
EP3715366A1 (fr) 2020-09-30
EP3360892A1 (fr) 2018-08-15
EP3360892B1 (fr) 2020-06-10
US20140113857A1 (en) 2014-04-24
EP2697254B1 (fr) 2018-06-06
EP2697254A4 (fr) 2014-12-17
US20210002336A1 (en) 2021-01-07
CA2833171C (fr) 2021-08-31
HK1255701A1 (zh) 2019-08-23
CN108276490B (zh) 2022-07-05
CN103649113A (zh) 2014-03-19
AU2012242502A1 (en) 2013-10-24
EP2697254A2 (fr) 2014-02-19
AU2012242502B2 (en) 2016-07-28
CN103649113B (zh) 2018-01-12
US20220204572A1 (en) 2022-06-30
WO2012142604A3 (fr) 2012-12-27
CA2833171A1 (fr) 2012-10-18
JP2014515748A (ja) 2014-07-03
CN108276490A (zh) 2018-07-13
US11220532B2 (en) 2022-01-11

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